11-32421536-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421536
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421536
    reference: chr 11
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.420C>G
  hgvsp: ENST00000379079.2:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.309C>G
  hgvsp: ENST00000527775.1:c.309C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.369C>G
  hgvsp: ENST00000530998.1:c.369C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-118C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*255C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.1005C>G
  hgvsp: ENST00000452863.3:c.1005C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1056C>G
  hgvsp: ENST00000332351.3:c.1056C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1056C>G
  hgvsp: ENST00000448076.3:c.1056C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.127C>G
  hgvsp: ENST00000527882.1:c.127C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala352Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-32421540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421540
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421540
    reference: chr 11
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.1001G>A
  hgvsp: ENSP00000415516.3:p.Gly334Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1052G>A
  hgvsp: ENSP00000413452.3:p.Gly351Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.123G>A
  hgvsp: ENSP00000435624.1:p.Gly42Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.305G>A
  hgvsp: ENSP00000435351.1:p.Gly102Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-122G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1052G>A
  hgvsp: ENSP00000331327.3:p.Gly351Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.365G>A
  hgvsp: ENSP00000435307.1:p.Gly122Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.416G>A
  hgvsp: ENSP00000368370.2:p.Gly139Glu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*251G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40755
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly351Glu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

11-32421544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421544
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421544
    reference: chr 11
allele count: 56
allele frequency: 4.624124719249571e-4
allele num: 121104
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.997T>C
  hgvsp: ENSP00000415516.3:p.Cys333Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.119T>C
  hgvsp: ENSP00000435624.1:p.Cys41Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.361T>C
  hgvsp: ENSP00000435307.1:p.Cys121Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*247T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1048T>C
  hgvsp: ENSP00000413452.3:p.Cys350Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-126T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.412T>C
  hgvsp: ENSP00000368370.2:p.Cys138Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1048T>C
  hgvsp: ENSP00000331327.3:p.Cys350Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance&not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.301T>C
  hgvsp: ENSP00000435351.1:p.Cys101Arg
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10799
  bin: 9.75e1
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys350Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-32421548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421548
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421548
    reference: chr 11
allele count: 3
allele frequency: 2.477373323644051e-5
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.297C>T
  hgvsp: ENST00000527775.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.115C>T
  hgvsp: ENST00000527882.1:c.115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.357C>T
  hgvsp: ENST00000530998.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-130C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1044C>T
  hgvsp: ENST00000332351.3:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1044C>T
  hgvsp: ENST00000448076.3:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*243C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.993C>T
  hgvsp: ENST00000452863.3:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.408C>T
  hgvsp: ENST00000379079.2:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile348Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

11-32421555-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421555
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421555
    reference: chr 11
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1037C>A
  hgvsp: ENSP00000413452.3:p.Thr346Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.108C>A
  hgvsp: ENSP00000435624.1:p.Thr37Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*236C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.986C>A
  hgvsp: ENSP00000415516.3:p.Thr329Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.401C>A
  hgvsp: ENSP00000368370.2:p.Thr134Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.350C>A
  hgvsp: ENSP00000435307.1:p.Thr117Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-137C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1037C>A
  hgvsp: ENSP00000331327.3:p.Thr346Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.290C>A
  hgvsp: ENSP00000435351.1:p.Thr97Lys
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr346Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

11-32421558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421558
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421558
    reference: chr 11
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.105C>T
  hgvsp: ENSP00000435624.1:p.Thr36Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1034C>T
  hgvsp: ENSP00000413452.3:p.Thr345Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.983C>T
  hgvsp: ENSP00000415516.3:p.Thr328Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.347C>T
  hgvsp: ENSP00000435307.1:p.Thr116Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-140C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1034C>T
  hgvsp: ENSP00000331327.3:p.Thr345Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.287C>T
  hgvsp: ENSP00000435351.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.398C>T
  hgvsp: ENSP00000368370.2:p.Thr133Ile
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*233C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr345Ile
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

11-32421569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421569
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421569
    reference: chr 11
allele count: 2
allele frequency: 1.654396558855158e-5
allele num: 120890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*222C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.336C>T
  hgvsp: ENST00000530998.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1023C>T
  hgvsp: ENST00000332351.3:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.276C>T
  hgvsp: ENST00000527775.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.94C>T
  hgvsp: ENST00000527882.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.387C>T
  hgvsp: ENST00000379079.2:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1023C>T
  hgvsp: ENST00000448076.3:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-151C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.972C>T
  hgvsp: ENST00000452863.3:c.972C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10750
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser341Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-32421572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421572
    reference: chr 11
allele count: 1
allele frequency: 8.277323444690924e-6
allele num: 120812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*219G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.333G>A
  hgvsp: ENST00000530998.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.273G>A
  hgvsp: ENST00000527775.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.91G>A
  hgvsp: ENST00000527882.1:c.91G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-154G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.384G>A
  hgvsp: ENST00000379079.2:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.969G>A
  hgvsp: ENST00000452863.3:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1020G>A
  hgvsp: ENST00000448076.3:c.1020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1020G>A
  hgvsp: ENST00000332351.3:c.1020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40151
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu340Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-32421574-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421574
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421574
    reference: chr 11
allele count: 2
allele frequency: 1.656259834042764e-5
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.382G>A
  hgvsp: ENSP00000368370.2:p.Glu128Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.331G>A
  hgvsp: ENSP00000435307.1:p.Glu111Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1018G>A
  hgvsp: ENSP00000413452.3:p.Glu340Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.967G>A
  hgvsp: ENSP00000415516.3:p.Glu323Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*217G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-156G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.271G>A
  hgvsp: ENSP00000435351.1:p.Glu91Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.89G>A
  hgvsp: ENSP00000435624.1:p.Glu31Lys
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1018G>A
  hgvsp: ENSP00000331327.3:p.Glu340Lys
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu340Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

11-32421585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421585
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421585
    reference: chr 11
allele count: 2
allele frequency: 1.663589026966778e-5
allele num: 120222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.320G>A
  hgvsp: ENSP00000435307.1:p.Ser107Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1007G>A
  hgvsp: ENSP00000413452.3:p.Ser336Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.956G>A
  hgvsp: ENSP00000415516.3:p.Ser319Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1007G>A
  hgvsp: ENSP00000331327.3:p.Ser336Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-167G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.260G>A
  hgvsp: ENSP00000435351.1:p.Ser87Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.78G>A
  hgvsp: ENSP00000435624.1:p.Ser27Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.371G>A
  hgvsp: ENSP00000368370.2:p.Ser124Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*206G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser336Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-32421587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421587
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421587
    reference: chr 11
allele count: 4
allele frequency: 3.330835206928137e-5
allele num: 120090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*204C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1005C>T
  hgvsp: ENST00000332351.3:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-169C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.76C>T
  hgvsp: ENST00000527882.1:c.76C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.318C>T
  hgvsp: ENST00000530998.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1005C>T
  hgvsp: ENST00000448076.3:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.258C>T
  hgvsp: ENST00000527775.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.369C>T
  hgvsp: ENST00000379079.2:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.954C>T
  hgvsp: ENST00000452863.3:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5026
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His335His
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

11-32421598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421598
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421598
    reference: chr 11
allele count: 1
allele frequency: 8.396587626788473e-6
allele num: 119096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-8G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-8G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26934
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1002-8G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

11-32421599-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421599
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421599
    reference: chr 11
allele count: 17
allele frequency: 1.428259371901937e-4
allele num: 119026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-9T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-9T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26645
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12966
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-32421602-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421602
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421602
    reference: chr 11
allele count: 8
allele frequency: 6.751054852320675e-5
allele num: 118500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-12T>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24702
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10749
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-32421605-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421605
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421605
    reference: chr 11
allele count: 4
allele frequency: 3.387533875338753e-5
allele num: 118080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-15T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-15T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23057
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29331
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

11-32421607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421607
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421607
    reference: chr 11
allele count: 1
allele frequency: 8.475007203756124e-6
allele num: 117994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-17C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-17C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-32421610-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421610
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421610
    reference: chr 11
allele count: 1
allele frequency: 8.54978540038645e-6
allele num: 116962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-20T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-20T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

11-32421611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421611
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421611
    reference: chr 11
allele count: 1
allele frequency: 8.548177528550913e-6
allele num: 116984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-21T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-21T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11373
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

11-32421612-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421612
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421612
    reference: chr 11
allele count: 1
allele frequency: 8.518758305789349e-6
allele num: 117388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-22T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-22T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4034
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

11-32421615-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421615
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421615
    reference: chr 11
allele count: 1
allele frequency: 8.590032126720154e-6
allele num: 116414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-25C>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13809
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

11-32421618-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421618
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421616
    reference: chr 11
allele count: 7
allele frequency: 6.013952369497234e-5
allele num: 116396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-30_73-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-30_951-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-30_315-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-30_-172-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-30_255-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-30_*201-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-30_1002-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-30_1002-29delTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-30_366-29delTG
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14312
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12860
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10749
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5696
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: TCA
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-32421619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421619
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421619
    reference: chr 11
allele count: 2
allele frequency: 1.720992668571232e-5
allele num: 116212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-29G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-29G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-32421622-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421622
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421622
    reference: chr 11
allele count: 3
allele frequency: 2.580378799607782e-5
allele num: 116262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-32A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-32A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5957
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

11-32421626-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32421626
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32421626
    reference: chr 11
allele count: 2
allele frequency: 1.741705129321606e-5
allele num: 114830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1002-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*201-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1002-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.315-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000436292
  ensembl transcript: ENST00000526685
  gene symbol: WT1
  hgvsc: ENST00000526685.1:c.-172-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.951-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.366-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.73-36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.255-36C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10746
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

11-32437991-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32437991
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32437991
    reference: chr 11
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1132T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+45T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+45T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+45T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+45T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+45T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+45T>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1132T>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43482
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57449
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-32437994-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32437994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32437994
    reference: chr 11
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1129C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+42C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+42C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+42C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+42C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+42C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+42C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1129C>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43482
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

11-32437995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32437995
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32437995
    reference: chr 11
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+41G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1128G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+41G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1128G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+41G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+41G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+41G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+41G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43482
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-32437999-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32437999
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32437999
    reference: chr 11
allele count: 14
allele frequency: 1.154353562005277e-4
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+37G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+37G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+37G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1124G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+37G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+37G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+37G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1124G>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43486
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

11-32437999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32437999
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32437999
    reference: chr 11
allele count: 5
allele frequency: 4.122691292875989e-5
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1124G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+37G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1124G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+37G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+37G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+37G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+37G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+37G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43486
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-32438000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438000
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438000
    reference: chr 11
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1123C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+36C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1123C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+36C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43478
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-32438001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438001
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438001
    reference: chr 11
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1122G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1122G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+35G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+35G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+35G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+35G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+35G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+35G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43478
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57448
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

11-32438008-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438008
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438008
    reference: chr 11
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+28G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+28G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1115G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+28G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+28G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+28G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1115G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+28G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57447
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

11-32438012-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438012
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438012
    reference: chr 11
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+24C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1111C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+24C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1111C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+24C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+24C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+24C>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+24C>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-32438016-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438016
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438016
    reference: chr 11
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+20A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+20A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1107A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+20A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+20A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+20A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1107A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+20A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43477
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-32438021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438021
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438021
    reference: chr 11
allele count: 3
allele frequency: 2.473981956424931e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1102C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+15C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+15C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1102C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+15C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+15C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+15C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+15C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43477
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

11-32438025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438025
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438025
    reference: chr 11
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+11A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+11A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+11A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1098A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+11A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+11A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1098A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+11A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43477
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

11-32438027-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438027
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438027
    reference: chr 11
allele count: 3
allele frequency: 2.473941153186436e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+9A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+9A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1096A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+9A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+9A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+9A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1096A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+9A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43477
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57447
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

11-32438032-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438032
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438032
    reference: chr 11
allele count: 2
allele frequency: 1.649294102124291e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*200+4A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.72+4A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1091A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1091A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.365+4A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.254+4A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.1001+4A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.1001+4A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43477
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1001+4A>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-32438039-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438039
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438039
    reference: chr 11
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.998G>A
  hgvsp: ENSP00000331327.3:p.Ser333Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*197G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1084G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.998G>A
  hgvsp: ENSP00000413452.3:p.Ser333Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.251G>A
  hgvsp: ENSP00000435351.1:p.Ser84Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1084G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.362G>A
  hgvsp: ENSP00000368370.2:p.Ser121Asn
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.69G>A
  hgvsp: ENSP00000435624.1:p.Ser24Asn
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43475
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser333Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

11-32438042-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438042
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438042
    reference: chr 11
allele count: 2
allele frequency: 1.649511744523621e-5
allele num: 121248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.66A>G
  hgvsp: ENSP00000435624.1:p.Gln23Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1081A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.995A>G
  hgvsp: ENSP00000331327.3:p.Gln332Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.359A>G
  hgvsp: ENSP00000368370.2:p.Gln120Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*194A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.248A>G
  hgvsp: ENSP00000435351.1:p.Gln83Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.995A>G
  hgvsp: ENSP00000413452.3:p.Gln332Arg
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1081A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43475
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln332Arg
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-32438056-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438056
    reference: chr 11
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.981A>G
  hgvsp: ENST00000332351.3:c.981A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*180A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.52A>G
  hgvsp: ENST00000527882.1:c.52A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.345A>G
  hgvsp: ENST00000379079.2:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.981A>G
  hgvsp: ENST00000448076.3:c.981A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1067A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.234A>G
  hgvsp: ENST00000527775.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1067A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43473
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys327Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

11-32438063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438063
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438063
    reference: chr 11
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.338C>T
  hgvsp: ENSP00000368370.2:p.Ser113Leu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.974C>T
  hgvsp: ENSP00000413452.3:p.Ser325Leu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.227C>T
  hgvsp: ENSP00000435351.1:p.Ser76Leu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.45C>T
  hgvsp: ENSP00000435624.1:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.974C>T
  hgvsp: ENSP00000331327.3:p.Ser325Leu
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*173C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1060C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1060C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43473
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser325Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

11-32438075-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438075
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438075
    reference: chr 11
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.962G>C
  hgvsp: ENSP00000331327.3:p.Gly321Ala
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.33G>C
  hgvsp: ENSP00000435624.1:p.Gly12Ala
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1048G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1048G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.215G>C
  hgvsp: ENSP00000435351.1:p.Gly72Ala
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.326G>C
  hgvsp: ENSP00000368370.2:p.Gly109Ala
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.962G>C
  hgvsp: ENSP00000413452.3:p.Gly321Ala
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*161G>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57446
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly321Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-32438075-CCAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438075
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438072
    reference: chr 11
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.323_325delCTG
  hgvsp: ENSP00000368370.2:p.Ala108del
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*158_*160delCTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.30_32delCTG
  hgvsp: ENSP00000435624.1:p.Ala11del
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.212_214delCTG
  hgvsp: ENSP00000435351.1:p.Ala71del
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1045_314+1047delCTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.959_961delCTG
  hgvsp: ENSP00000331327.3:p.Ala320del
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1045_950+1047delCTG
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.959_961delCTG
  hgvsp: ENSP00000413452.3:p.Ala320del
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala320del
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: CCAG
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

11-32438087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438087
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438087
    reference: chr 11
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-1G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1036G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-1G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-1G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-1G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-1G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-1G>A
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1036G>A
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57445
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: c.951-1G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-32438099-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438099
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438099
    reference: chr 11
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1024T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-13T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-13T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1024T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-13T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-13T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-13T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-13T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43471
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-32438106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438106
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438106
    reference: chr 11
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-20C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1017C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-20C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-20C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-20C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1017C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-20C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-20C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

11-32438108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438108
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438108
    reference: chr 11
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-22C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1015C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-22C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1015C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-22C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-22C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-22C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-22C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-32438112-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438112
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438112
    reference: chr 11
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-26A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-26A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-26A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-26A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-26A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+1011A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-26A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+1011A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

11-32438128-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438128
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438128
    reference: chr 11
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+995G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-42G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+995G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-42G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-42G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-42G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-42G>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-42G>C
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-32438130-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438130
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32438130
    reference: chr 11
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*150-44A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.315-44A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+993A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.951-44A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.951-44A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.204-44A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+993A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.22-44A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 6.25e1
  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: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-32439073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439073
    reference: chr 11
allele count: 2
allele frequency: 1.665806000233213e-5
allele num: 120062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+50T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+50T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+50T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+50T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+50T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*46T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+50T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+50T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10976
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6861
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

11-32439075-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439075
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439075
    reference: chr 11
allele count: 2
allele frequency: 1.664946222237022e-5
allele num: 120124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+48T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+48T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+48T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*44T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+48T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+48T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+48T>C
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+48T>C
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15992
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-32439076-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439076
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439076
    reference: chr 11
allele count: 2
allele frequency: 1.666444474070124e-5
allele num: 120016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+47G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+47G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+47G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+47G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+47G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+47G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*43G>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+47G>T
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24252
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

11-32439078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439078
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439078
    reference: chr 11
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+45C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+45C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+45C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+45C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+45C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*41C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+45C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+45C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25422
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10966
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

11-32439078-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439078
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439078
    reference: chr 11
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+45C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+45C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+45C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+45C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+45C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*41C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+45C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+45C>G
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6837
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-32439098-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439098
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439098
    reference: chr 11
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+25C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+25C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+25C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+25C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+25C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*21C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+25C>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+25C>T
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-32439098-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439098
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439098
    reference: chr 11
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*21C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+25C>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+25C>G
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20879
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10956
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

11-32439103-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439103
    reference: chr 11
allele count: 1
allele frequency: 8.278008642241022e-6
allele num: 120802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+20A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+20A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*16A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+20A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+20A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+20A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+20A>T
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+20A>T
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-32439107-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439107
    reference: chr 11
allele count: 1
allele frequency: 8.269930532583527e-6
allele num: 120920
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*12T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+16T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+16T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+16T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+16T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+16T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+16T>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+16T>G
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

11-32439108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32439108
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 32439108
    reference: chr 11
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368370
  ensembl transcript: ENST00000379079
  gene symbol: WT1
  hgvsc: ENST00000379079.2:c.314+15A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435351
  ensembl transcript: ENST00000527775
  gene symbol: WT1
  hgvsc: ENST00000527775.1:c.203+15A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000368368
  ensembl transcript: ENST00000379077
  gene symbol: WT1
  hgvsc: ENST00000379077.3:c.*11A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435624
  ensembl transcript: ENST00000527882
  gene symbol: WT1
  hgvsc: ENST00000527882.1:c.21+15A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000415516
  ensembl transcript: ENST00000452863
  gene symbol: WT1
  hgvsc: ENST00000452863.3:c.950+15A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000413452
  ensembl transcript: ENST00000448076
  gene symbol: WT1
  hgvsc: ENST00000448076.3:c.950+15A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000331327
  ensembl transcript: ENST00000332351
  gene symbol: WT1
  hgvsc: ENST00000332351.3:c.950+15A>G
  variant of: http://identifiers.org/hgnc/12796
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184937
  ensembl protein: ENSP00000435307
  ensembl transcript: ENST00000530998
  gene symbol: WT1
  hgvsc: ENST00000530998.1:c.314+15A>G
  variant of: http://identifiers.org/hgnc/12796
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

14-55453912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453912
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453912
    reference: chr 14
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*170G>A
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1351G>A
  hgvsp: ENSP00000391049.1:p.Val451Met
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1720G>A
  hgvsp: ENSP00000353793.3:p.Val574Met
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.274G>A
  hgvsp: ENSP00000352085.4:p.Val92Met
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1351G>A
  hgvsp: ENSP00000399349.2:p.Val451Met
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3848
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val574Met
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-55453915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453915
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453915
    reference: chr 14
allele count: 4
allele frequency: 3.297011259293451e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*167G>A
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1717G>A
  hgvsp: ENSP00000353793.3:p.Val573Met
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1348G>A
  hgvsp: ENSP00000391049.1:p.Val450Met
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1348G>A
  hgvsp: ENSP00000399349.2:p.Val450Met
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.271G>A
  hgvsp: ENSP00000352085.4:p.Val91Met
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val573Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

14-55453921-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453921
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453921
    reference: chr 14
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1342G>A
  hgvsp: ENSP00000399349.2:p.Gly448Arg
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1342G>A
  hgvsp: ENSP00000391049.1:p.Gly448Arg
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.265G>A
  hgvsp: ENSP00000352085.4:p.Gly89Arg
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*161G>A
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1711G>A
  hgvsp: ENSP00000353793.3:p.Gly571Arg
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35590
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11389
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3046
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly571Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

14-55453925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453925
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453925
    reference: chr 14
allele count: 3
allele frequency: 2.47255464345762e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1338T>C
  hgvsp: ENST00000421192.1:c.1338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.261T>C
  hgvsp: ENST00000359167.4:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1707T>C
  hgvsp: ENST00000360586.3:c.1707T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1338T>C
  hgvsp: ENST00000420358.2:c.1338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*157T>C
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35600
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu569Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

14-55453934-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453934
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453934
    reference: chr 14
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*148A>G
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1329A>G
  hgvsp: ENST00000420358.2:c.1329A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1329A>G
  hgvsp: ENST00000421192.1:c.1329A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1698A>G
  hgvsp: ENST00000360586.3:c.1698A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.252A>G
  hgvsp: ENST00000359167.4:c.252A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3842
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val566Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

14-55453943-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453943
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453943
    reference: chr 14
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1320A>T
  hgvsp: ENSP00000399349.2:p.Gln440His
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1320A>T
  hgvsp: ENSP00000391049.1:p.Gln440His
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.243A>T
  hgvsp: ENSP00000352085.4:p.Gln81His
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1689A>T
  hgvsp: ENSP00000353793.3:p.Gln563His
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*139A>T
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3046
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11408
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln563His
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: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

14-55453948-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453948
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453948
    reference: chr 14
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.238G>A
  hgvsp: ENSP00000352085.4:p.Val80Ile
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1315G>A
  hgvsp: ENSP00000399349.2:p.Val439Ile
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1684G>A
  hgvsp: ENSP00000353793.3:p.Val562Ile
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*134G>A
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1315G>A
  hgvsp: ENSP00000391049.1:p.Val439Ile
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3839
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1843
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val562Ile
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

14-55453960-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453960
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453960
    reference: chr 14
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1303A>G
  hgvsp: ENSP00000399349.2:p.Thr435Ala
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1672A>G
  hgvsp: ENSP00000353793.3:p.Thr558Ala
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1303A>G
  hgvsp: ENSP00000391049.1:p.Thr435Ala
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.226A>G
  hgvsp: ENSP00000352085.4:p.Thr76Ala
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*122A>G
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr558Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-55453968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453968
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453968
    reference: chr 14
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1295G>A
  hgvsp: ENSP00000391049.1:p.Arg432Gln
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1295G>A
  hgvsp: ENSP00000399349.2:p.Arg432Gln
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1664G>A
  hgvsp: ENSP00000353793.3:p.Arg555Gln
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.218G>A
  hgvsp: ENSP00000352085.4:p.Arg73Gln
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg555Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

14-55453969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55453969
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 55453969
    reference: chr 14
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000391049
  ensembl transcript: ENST00000421192
  gene symbol: WDHD1
  hgvsc: ENST00000421192.1:c.1294C>T
  hgvsp: ENSP00000391049.1:p.Arg432Ter
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000399349
  ensembl transcript: ENST00000420358
  gene symbol: WDHD1
  hgvsc: ENST00000420358.2:c.1294C>T
  hgvsp: ENSP00000399349.2:p.Arg432Ter
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000352085
  ensembl transcript: ENST00000359167
  gene symbol: WDHD1
  hgvsc: ENST00000359167.4:c.217C>T
  hgvsp: ENSP00000352085.4:p.Arg73Ter
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000353793
  ensembl transcript: ENST00000360586
  gene symbol: WDHD1
  hgvsc: ENST00000360586.3:c.1663C>T
  hgvsp: ENSP00000353793.3:p.Arg555Ter
  variant of: http://identifiers.org/hgnc/23170
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198554
  ensembl protein: ENSP00000456806
  ensembl transcript: ENST00000567693
  gene symbol: WDHD1
  hgvsc: ENST00000567693.1:c.*113C>T
  variant of: http://identifiers.org/hgnc/23170
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12015
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg555Ter
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5237
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 212
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10754
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 7.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

DP
type: SiteQuality
SIO_000300: 2.292391e6

FS
type: SiteQuality
SIO_000300: 3.503e0

QD
type: SiteQuality
SIO_000300: 1.161e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.206e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.78e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 558
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.339e0

QD
type: SiteQuality
SIO_000300: 1.039e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.118e0

DP
type: SiteQuality
SIO_000300: 2.292631e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

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

Latino
type: Population
allele count: 9
allele frequency: 7.796257796257797e-4
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 6.600660066006601e-4
allele num: 66660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.217e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.294956e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.473e0

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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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.732501732501733e-4
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

QD
type: SiteQuality
SIO_000300: 1.201e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.326e0

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

DP
type: SiteQuality
SIO_000300: 2.292668e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 10749
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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: 16394
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.292454e6

QD
type: SiteQuality
SIO_000300: 3.168e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.246e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.325e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.291954e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 1.256e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.65e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.514e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.929012345679012e-4
allele num: 10368
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 9.93e0

DP
type: SiteQuality
SIO_000300: 2.289291e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.645e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.458e0

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: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e0

FS
type: SiteQuality
SIO_000300: 9.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

DP
type: SiteQuality
SIO_000300: 2.287467e6

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.124e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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: 1
allele frequency: 1.504211793020457e-5
allele num: 66480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.416e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 1.958e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

DP
type: SiteQuality
SIO_000300: 2.286495e6

GenotypeQuality
all individuals: 38637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10750
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020418025854778e-5
allele num: 66216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
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: 10304
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.149e1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.602e0

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 2.273646e6

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 911
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variant carriers: 0

GenotypeQuality
all individuals: 10751
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variant carriers: 4

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.914319020788809e-4
allele num: 10294
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.756567425569177e-5
allele num: 11420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.269413e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.229e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.554e0

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.56e-1

GenotypeQuality
all individuals: 10749
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16130
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.800078400627205e-5
allele num: 10204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0307e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 1.006e1

VQSLOD
type: SiteQuality
SIO_000300: -1.491e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.23541e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.37e0

GenotypeQuality
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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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
all individuals: 10761
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variant carriers: 17

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3281
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variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.720238095238095e-4
allele num: 16128
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.170138076293003e-3
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526111772426212e-5
allele num: 65526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.354e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 2.231176e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 1.392e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 4461
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variant carriers: 0

GenotypeQuality
all individuals: 1030
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variant carriers: 0

GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 634
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variant carriers: 0

GenotypeQuality
all individuals: 351
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GenotypeQuality
all individuals: 1056
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GenotypeQuality
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GenotypeQuality
all individuals: 4299
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GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 31793
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variant carriers: 0

GenotypeQuality
all individuals: 493
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variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.967709885742673e-4
allele num: 16104
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65190
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.247e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

DP
type: SiteQuality
SIO_000300: 2.205972e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.77e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
SIO_000300: 1.588e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 2489
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10751
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 971
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GenotypeQuality
all individuals: 429
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GenotypeQuality
all individuals: 195
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GenotypeQuality
all individuals: 1377
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GenotypeQuality
all individuals: 761
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 1948
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GenotypeQuality
all individuals: 5088
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variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.159342182254935e-5
allele num: 64942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

QD
type: SiteQuality
SIO_000300: 1.61e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

DP
type: SiteQuality
SIO_000300: 2.183247e6

VQSLOD
type: SiteQuality
SIO_000300: 5.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4168
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1374
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GenotypeQuality
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GenotypeQuality
all individuals: 454
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GenotypeQuality
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GenotypeQuality
all individuals: 239
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 5126
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64890
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.178967224711153e-4
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.486e0

FS
type: SiteQuality
SIO_000300: 3.59e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

DP
type: SiteQuality
SIO_000300: 2.183732e6

GenotypeQuality
all individuals: 10745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 828
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GenotypeQuality
all individuals: 2594
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variant carriers: 0

GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 934
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 774
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GenotypeQuality
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GenotypeQuality
all individuals: 183
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variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55574224462491e-5
allele num: 64278
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.427e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

DP
type: SiteQuality
SIO_000300: 2.152971e6

GenotypeQuality
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GenotypeQuality
all individuals: 752
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GenotypeQuality
all individuals: 2068
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GenotypeQuality
all individuals: 136
bin: 1.75e1
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 26063
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GenotypeQuality
all individuals: 935
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GenotypeQuality
all individuals: 6319
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GenotypeQuality
all individuals: 752
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GenotypeQuality
all individuals: 182
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GenotypeQuality
all individuals: 3837
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GenotypeQuality
all individuals: 10746
bin: 9.75e1
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GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555258328408349e-5
allele num: 64298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 2.1524e6

VQSLOD
type: SiteQuality
SIO_000300: -1.672e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.641e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 5.827e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549907005579665e-5
allele num: 64520
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.984e-1

FS
type: SiteQuality
SIO_000300: 6.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

QD
type: SiteQuality
SIO_000300: 1.724e1

MQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

DP
type: SiteQuality
SIO_000300: 2.139613e6

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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562402349853134e-5
allele num: 64004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15854
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.171e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.073513e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.784056508577195e-4
allele num: 15856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63998
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.202790473899447e-4
allele num: 8314
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.067e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 6.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 2.067618e6

QD
type: SiteQuality
SIO_000300: 1.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.69e-1

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10940
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.12930279133809e-5
allele num: 63912
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.066722e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.139e0

VQSLOD
type: SiteQuality
SIO_000300: -1.393e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 307
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.610977371208474e-4
allele num: 8308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.093e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.055243e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

QD
type: SiteQuality
SIO_000300: 1.147e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

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
all individuals: 913
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.275347532202525e-4
allele num: 15682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63176
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

DP
type: SiteQuality
SIO_000300: 1.997477e6

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.002e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.711e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.192e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

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

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

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

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

Other
type: Population
allele count: 0
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allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.484e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.98e1

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
all individuals: 62
bin: 4.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.412e1

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
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: 66672
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.945002e6

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.75e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 3.99e0

QD
type: SiteQuality
SIO_000300: 1.346e1

VQSLOD
type: SiteQuality
SIO_000300: -8.241000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 312
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 12
allele frequency: 7.26920281075842e-4
allele num: 16508
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

FS
type: SiteQuality
SIO_000300: 1.964e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.241e0

DP
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SIO_000300: 6.945564e6

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

QD
type: SiteQuality
SIO_000300: 1.377e1

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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bin: 9.75e1
variant carriers: 5

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

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

African
type: Population
allele count: 2
allele frequency: 1.92975685063682e-4
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.964e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
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SIO_000300: -2.241e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.377e1

DP
type: SiteQuality
SIO_000300: 6.945564e6

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.892e1

DP
type: SiteQuality
SIO_000300: 6.943057e6

FS
type: SiteQuality
SIO_000300: 4.427e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.348e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.142e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.446e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.844e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

DP
type: SiteQuality
SIO_000300: 6.943075e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.374e0

GenotypeQuality
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variant carriers: 0

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

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: 10358
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.73e-1

MQ
type: SiteQuality
SIO_000300: 5.995e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.535e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.911e0

QD
type: SiteQuality
SIO_000300: 1.485e1

DP
type: SiteQuality
SIO_000300: 6.943218e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

Other
type: Population
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allele num: 908
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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

South Asian
type: Population
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.59e-1

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

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
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MQRankSum
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DP
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.2315e1

BaseQRankSum
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SIO_000300: 9.06e0

QD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 2.594258042199931e-4
allele num: 11564
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 908
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
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ReadPosRankSum
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SIO_000300: 1.14e0

FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.499640028797696e-5
allele num: 66672
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MQ
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SIO_000300: 5.964e1

FS
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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SIO_000300: 6.942771e6

MQRankSum
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ClippingRankSum
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SIO_000300: -1.886e0

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

Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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allele frequency: 0.0e0
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South Asian
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allele num: 16508
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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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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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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MQ
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SIO_000300: 5.955e1

FS
type: SiteQuality
SIO_000300: 3.74e-1

ReadPosRankSum
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SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.064e1

InbreedingCoeff
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SIO_000300: -1.0e-4

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10348
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele frequency: 1.21153380179307e-4
allele num: 16508
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.93e-1

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

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

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
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
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.938391e6

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 1.507e0

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.397e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.546e0

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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bin: 4.75e1
variant carriers: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

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

QD
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FS
type: SiteQuality
SIO_000300: 4.597e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.91e0

MQRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-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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variant carriers: 0

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

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16502
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African
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allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.503e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

FS
type: SiteQuality
SIO_000300: 1.143e0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

DP
type: SiteQuality
SIO_000300: 6.935084e6

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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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.215e0

DP
type: SiteQuality
SIO_000300: 6.934876e6

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

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.005e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.705e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.03e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.674e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.164e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.693e0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: -2.243e0

MQ
type: SiteQuality
SIO_000300: 5.844e1

QD
type: SiteQuality
SIO_000300: 1.31e1

DP
type: SiteQuality
SIO_000300: 6.933906e6

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
all individuals: 326
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
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: 16490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 6.930616e6

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.622e0

QD
type: SiteQuality
SIO_000300: 1.648e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 6.403e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.930309e6

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.445e1

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032508491023775e-5
allele num: 65952
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.968242e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-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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variant carriers: 0

African
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allele count: 2
allele frequency: 1.935733643050716e-4
allele num: 10332
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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Other
type: Population
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num of homozygotes: 0

East 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: 6572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65970
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65908
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele num: 16364
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: 2.23e-1

MQRankSum
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MQ
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 8.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

African
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allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6574
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MQRankSum
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

African
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allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-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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variant carriers: 1

African
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allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66234
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
allele num: 8598
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South Asian
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allele frequency: 6.091617933723197e-5
allele num: 16416
num of homozygotes: 0

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

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

QD
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MQRankSum
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BaseQRankSum
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SIO_000300: -2.171e0

ReadPosRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.058e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

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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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

European (Finnish)
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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: 8598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.035338e6

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

FS
type: SiteQuality
SIO_000300: 7.058e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.229e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.171e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.541e1

DP
type: SiteQuality
SIO_000300: 2.044109e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
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African
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allele frequency: 0.0e0
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East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8628
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Other
type: Population
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

Other
type: Population
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South Asian
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East Asian
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allele frequency: 0.0e0
allele num: 8628
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
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Other
type: Population
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African
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allele num: 10386
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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

European (Non-Finnish)
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allele frequency: 5.997001499250375e-5
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East Asian
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African
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Latino
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allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

Other
type: Population
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allele num: 908
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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MQ
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.148385e6

MQRankSum
type: SiteQuality
SIO_000300: -1.628e0

FS
type: SiteQuality
SIO_000300: 1.047e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.055e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.521e0

VQSLOD
type: SiteQuality
SIO_000300: -1.764e0

MQ
type: SiteQuality
SIO_000300: 5.621e1

QD
type: SiteQuality
SIO_000300: 1.12e1

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

African
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allele count: 3
allele frequency: 2.886836027713626e-4
allele num: 10392
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 2.148642e6

QD
type: SiteQuality
SIO_000300: 1.371e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

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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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.711e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

QD
type: SiteQuality
SIO_000300: 1.206e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 2.149044e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.121e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
SIO_000300: 2.149353e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.508e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.83e1

DP
type: SiteQuality
SIO_000300: 2.149716e6

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.071e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.425e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.835e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3050
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 2.647e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e0

VQSLOD
type: SiteQuality
SIO_000300: -2.761e0

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e0

DP
type: SiteQuality
SIO_000300: 2.150198e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 2.150379e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

FS
type: SiteQuality
SIO_000300: 6.704e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.459e1

VQSLOD
type: SiteQuality
SIO_000300: 5.76e-1