2-63631692-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631692
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631692
    reference: chr 2
allele count: 3
allele frequency: 2.489213408562894e-5
allele num: 120520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1037A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.287A>T
  hgvsp: ENSP00000386795.2:p.Asp96Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.350A>T
  hgvsp: ENSP00000386592.1:p.Asp117Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.449A>T
  hgvsp: ENSP00000381552.3:p.Asp150Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1173A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.926A>T
  hgvsp: ENSP00000387222.3:p.Asp309Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.926A>T
  hgvsp: ENSP00000272321.7:p.Asp309Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.350A>T
  hgvsp: ENSP00000386769.1:p.Asp117Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.628A>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7815
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp309Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-63631693-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631693
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631693
    reference: chr 2
allele count: 1
allele frequency: 8.298479718515568e-6
allele num: 120504
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.925G>C
  hgvsp: ENSP00000272321.7:p.Asp309His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1036G>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.349G>C
  hgvsp: ENSP00000386592.1:p.Asp117His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.286G>C
  hgvsp: ENSP00000386795.2:p.Asp96His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1172G>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.925G>C
  hgvsp: ENSP00000387222.3:p.Asp309His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.448G>C
  hgvsp: ENSP00000381552.3:p.Asp150His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.349G>C
  hgvsp: ENSP00000386769.1:p.Asp117His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.627G>C
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp309His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

2-63631694-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631694
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631694
    reference: chr 2
allele count: 71
allele frequency: 5.891138400265516e-4
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.348A>G
  hgvsp: ENST00000409120.1:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1171A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.626A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.924A>G
  hgvsp: ENST00000272321.7:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.285A>G
  hgvsp: ENST00000409354.2:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.348A>G
  hgvsp: ENST00000409199.1:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.924A>G
  hgvsp: ENST00000409562.3:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.447A>G
  hgvsp: ENST00000398544.3:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1035A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 31670
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6069
  bin: 9.75e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val308Val
num of homozygotes: 2
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-63631700-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631700
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631701
    reference: chr 2
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.278dupT
  hgvsp: ENSP00000386795.2:p.Ser94LysfsTer9
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1028dupT
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.341dupT
  hgvsp: ENSP00000386769.1:p.Ser115LysfsTer9
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.440dupT
  hgvsp: ENSP00000381552.3:p.Ser148LysfsTer9
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.917dupT
  hgvsp: ENSP00000272321.7:p.Ser307LysfsTer9
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.341dupT
  hgvsp: ENSP00000386592.1:p.Ser115LysfsTer9
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.917dupT
  hgvsp: ENSP00000387222.3:p.Ser307LysfsTer9
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.619dupT
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1164dupT
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser307LysfsTer9
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

2-63631702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631702
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631702
    reference: chr 2
allele count: 2
allele frequency: 1.659806134643474e-5
allele num: 120496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.618G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1027G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.340G>A
  hgvsp: ENSP00000386769.1:p.Val114Ile
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.439G>A
  hgvsp: ENSP00000381552.3:p.Val147Ile
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.916G>A
  hgvsp: ENSP00000272321.7:p.Val306Ile
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.916G>A
  hgvsp: ENSP00000387222.3:p.Val306Ile
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.340G>A
  hgvsp: ENSP00000386592.1:p.Val114Ile
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1163G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.277G>A
  hgvsp: ENSP00000386795.2:p.Val93Ile
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val306Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-63631703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631703
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631703
    reference: chr 2
allele count: 4
allele frequency: 3.319612269286947e-5
allele num: 120496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.339C>T
  hgvsp: ENST00000409120.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.438C>T
  hgvsp: ENST00000398544.3:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1162C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.339C>T
  hgvsp: ENST00000409199.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.915C>T
  hgvsp: ENST00000409562.3:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.915C>T
  hgvsp: ENST00000272321.7:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1026C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.276C>T
  hgvsp: ENST00000409354.2:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.617C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser305Ser
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

2-63631706-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631706
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631706
    reference: chr 2
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.435C>G
  hgvsp: ENSP00000381552.3:p.His145Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.912C>G
  hgvsp: ENSP00000272321.7:p.His304Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.336C>G
  hgvsp: ENSP00000386769.1:p.His112Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1159C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.912C>G
  hgvsp: ENSP00000387222.3:p.His304Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*1023C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.336C>G
  hgvsp: ENSP00000386592.1:p.His112Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.273C>G
  hgvsp: ENSP00000386795.2:p.His91Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.614C>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His304Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

2-63631738-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631738
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631738
    reference: chr 2
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.241A>G
  hgvsp: ENSP00000386795.2:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.880A>G
  hgvsp: ENSP00000272321.7:p.Lys294Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1127A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.304A>G
  hgvsp: ENSP00000386592.1:p.Lys102Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*991A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.304A>G
  hgvsp: ENSP00000386769.1:p.Lys102Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.403A>G
  hgvsp: ENSP00000381552.3:p.Lys135Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.880A>G
  hgvsp: ENSP00000387222.3:p.Lys294Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.582A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys294Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

2-63631740-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631740
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631740
    reference: chr 2
allele count: 1
allele frequency: 8.298479718515568e-6
allele num: 120504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1125C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.878C>G
  hgvsp: ENSP00000387222.3:p.Thr293Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*989C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.302C>G
  hgvsp: ENSP00000386769.1:p.Thr101Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.401C>G
  hgvsp: ENSP00000381552.3:p.Thr134Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.302C>G
  hgvsp: ENSP00000386592.1:p.Thr101Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.580C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.878C>G
  hgvsp: ENSP00000272321.7:p.Thr293Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.239C>G
  hgvsp: ENSP00000386795.2:p.Thr80Ser
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr293Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

2-63631749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631749
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631749
    reference: chr 2
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.869G>A
  hgvsp: ENSP00000272321.7:p.Arg290His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.571G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.230G>A
  hgvsp: ENSP00000386795.2:p.Arg77His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.293G>A
  hgvsp: ENSP00000386769.1:p.Arg98His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.293G>A
  hgvsp: ENSP00000386592.1:p.Arg98His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.392G>A
  hgvsp: ENSP00000381552.3:p.Arg131His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1116G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.869G>A
  hgvsp: ENSP00000387222.3:p.Arg290His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*980G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6062
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg290His
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-63631750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631750
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631750
    reference: chr 2
allele count: 44
allele frequency: 3.652786079564322e-4
allele num: 120456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.292C>T
  hgvsp: ENSP00000386592.1:p.Arg98Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1115C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*979C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.868C>T
  hgvsp: ENSP00000387222.3:p.Arg290Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.391C>T
  hgvsp: ENSP00000381552.3:p.Arg131Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.292C>T
  hgvsp: ENSP00000386769.1:p.Arg98Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.868C>T
  hgvsp: ENSP00000272321.7:p.Arg290Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.570C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.229C>T
  hgvsp: ENSP00000386795.2:p.Arg77Cys
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14242
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg290Cys
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

2-63631755-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631755
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631755
    reference: chr 2
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.386A>C
  hgvsp: ENSP00000381552.3:p.Asp129Ala
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.863A>C
  hgvsp: ENSP00000272321.7:p.Asp288Ala
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*974A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1110A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.287A>C
  hgvsp: ENSP00000386592.1:p.Asp96Ala
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.863A>C
  hgvsp: ENSP00000387222.3:p.Asp288Ala
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.287A>C
  hgvsp: ENSP00000386769.1:p.Asp96Ala
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.565A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.224A>C
  hgvsp: ENSP00000386795.2:p.Asp75Ala
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp288Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

2-63631762-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631762
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631762
    reference: chr 2
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.217C>A
  hgvsp: ENSP00000386795.2:p.Pro73Thr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.856C>A
  hgvsp: ENSP00000272321.7:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.280C>A
  hgvsp: ENSP00000386769.1:p.Pro94Thr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1103C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*967C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.280C>A
  hgvsp: ENSP00000386592.1:p.Pro94Thr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.856C>A
  hgvsp: ENSP00000387222.3:p.Pro286Thr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.558C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.379C>A
  hgvsp: ENSP00000381552.3:p.Pro127Thr
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro286Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

2-63631764-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631764
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631764
    reference: chr 2
allele count: 1
allele frequency: 8.313795912937929e-6
allele num: 120282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.377A>G
  hgvsp: ENSP00000381552.3:p.Asp126Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.854A>G
  hgvsp: ENSP00000272321.7:p.Asp285Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.215A>G
  hgvsp: ENSP00000386795.2:p.Asp72Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1101A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.278A>G
  hgvsp: ENSP00000386769.1:p.Asp93Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.854A>G
  hgvsp: ENSP00000387222.3:p.Asp285Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.278A>G
  hgvsp: ENSP00000386592.1:p.Asp93Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*965A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.556A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8004
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp285Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

2-63631776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631776
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631776
    reference: chr 2
allele count: 7
allele frequency: 5.828573331779047e-5
allele num: 120098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.365G>A
  hgvsp: ENSP00000381552.3:p.Arg122His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.203G>A
  hgvsp: ENSP00000386795.2:p.Arg68His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.266G>A
  hgvsp: ENSP00000386769.1:p.Arg89His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.842G>A
  hgvsp: ENSP00000272321.7:p.Arg281His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.544G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.842G>A
  hgvsp: ENSP00000387222.3:p.Arg281His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.266G>A
  hgvsp: ENSP00000386592.1:p.Arg89His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1089G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*953G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg281His
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: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

2-63631777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631777
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631777
    reference: chr 2
allele count: 1
allele frequency: 8.328752519447637e-6
allele num: 120066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.543C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*952C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.841C>T
  hgvsp: ENSP00000387222.3:p.Arg281Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.202C>T
  hgvsp: ENSP00000386795.2:p.Arg68Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1088C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.265C>T
  hgvsp: ENSP00000386592.1:p.Arg89Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.841C>T
  hgvsp: ENSP00000272321.7:p.Arg281Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.265C>T
  hgvsp: ENSP00000386769.1:p.Arg89Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.364C>T
  hgvsp: ENSP00000381552.3:p.Arg122Cys
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7988
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg281Cys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

2-63631781-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631781
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631781
    reference: chr 2
allele count: 4
allele frequency: 3.336169077048825e-5
allele num: 119898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.198T>C
  hgvsp: ENST00000409354.2:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1084T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.261T>C
  hgvsp: ENST00000409199.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.837T>C
  hgvsp: ENST00000272321.7:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.539T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*948T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.837T>C
  hgvsp: ENST00000409562.3:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.261T>C
  hgvsp: ENST00000409120.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.360T>C
  hgvsp: ENST00000398544.3:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6088
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30710
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser279Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

2-63631793-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631793
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631793
    reference: chr 2
allele count: 1
allele frequency: 8.368621018628551e-6
allele num: 119494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-1G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-1G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6092
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 7.75e1
  variant carriers: 0
hgvs: c.826-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-63631800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631800
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631800
    reference: chr 2
allele count: 1
allele frequency: 8.38335401227323e-6
allele num: 119284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-8C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-8C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
hgvs: c.826-8C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

2-63631800-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631800
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631800
    reference: chr 2
allele count: 13
allele frequency: 1.08983602159552e-4
allele num: 119284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-8C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-8C>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30582
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13823
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6102
  bin: 9.75e1
  variant carriers: 13
hgvs: c.826-8C>A
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

2-63631805-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631805
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631805
    reference: chr 2
allele count: 6
allele frequency: 5.035500276952515e-5
allele num: 119154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-13T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-13T>C
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-63631806-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631806
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631806
    reference: chr 2
allele count: 2
allele frequency: 1.679063754050741e-5
allele num: 119114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-14A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-14A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13759
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7917
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

2-63631808-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631808
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631808
    reference: chr 2
allele count: 2
allele frequency: 1.681831177786374e-5
allele num: 118918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-16A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-16A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3414
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

2-63631812-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631812
    reference: chr 2
allele count: 1
allele frequency: 8.410287463625507e-6
allele num: 118902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-20C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-20C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3410
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

2-63631812-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631812
    reference: chr 2
allele count: 2
allele frequency: 1.682057492725101e-5
allele num: 118902
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-20C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-20C>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30089
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-63631818-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631818
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631818
    reference: chr 2
allele count: 1
allele frequency: 8.425877555147369e-6
allele num: 118682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-26A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-26A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

2-63631819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631819
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631819
    reference: chr 2
allele count: 23
allele frequency: 1.937657961246841e-4
allele num: 118700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-27G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-27G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4547
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-63631828-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631828
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631828
    reference: chr 2
allele count: 2
allele frequency: 1.688590196045322e-5
allele num: 118442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-36A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-36A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28188
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6112
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-63631830-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631830
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631830
    reference: chr 2
allele count: 23503
allele frequency: 1.986191393705845e-1
allele num: 118332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-38A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-38A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 4.75e1
  variant carriers: 2266
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 5.75e1
  variant carriers: 2185
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.75e1
  variant carriers: 365
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 5.25e1
  variant carriers: 2439
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.25e1
  variant carriers: 1011
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 2.75e1
  variant carriers: 714
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.25e1
  variant carriers: 306
genotype depth: GenotypeDepth
  all individuals: 19555
  bin: 2.25e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 6.25e1
  variant carriers: 1907
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.75e1
  variant carriers: 317
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 4.25e1
  variant carriers: 2061
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 1550
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.75e1
  variant carriers: 1454
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 459
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 9.75e1
  variant carriers: 1411
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 740
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 3.25e1
  variant carriers: 1090
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 45
num of homozygotes: 2598
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

2-63631832-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631832
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631832
    reference: chr 2
allele count: 2
allele frequency: 1.693222032205083e-5
allele num: 118118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-40C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-40C>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20512
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-63631836-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631836
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631836
    reference: chr 2
allele count: 1
allele frequency: 8.490261669864665e-6
allele num: 117782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-44A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-44A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

2-63631839-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631839
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631839
    reference: chr 2
allele count: 9
allele frequency: 7.643182281404987e-5
allele num: 117752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-47A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-47A>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19885
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6201
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-63631839-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63631839
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63631839
    reference: chr 2
allele count: 1
allele frequency: 8.492424757116652e-6
allele num: 117752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.187-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*937-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.250-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1073-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.528-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.250-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.826-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.349-47A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.826-47A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19275
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

2-63660842-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660842
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660842
    reference: chr 2
allele count: 1
allele frequency: 1.52522725886157e-5
allele num: 65564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.186+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.348+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.825+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.527+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*936+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.249+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.825+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1072+37G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.249+37G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-63660847-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660847
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660847
    reference: chr 2
allele count: 7
allele frequency: 9.852494088503547e-5
allele num: 71048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.249+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*936+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1072+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.825+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.825+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.348+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.249+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.186+32A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.527+32A>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-63660849-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660849
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660849
    reference: chr 2
allele count: 5
allele frequency: 6.734006734006734e-5
allele num: 74250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.249+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.825+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.348+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.186+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*936+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.249+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1072+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.825+30A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.527+30A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22734
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

2-63660859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660859
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660859
    reference: chr 2
allele count: 2
allele frequency: 2.108014671782116e-5
allele num: 94876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.249+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.348+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.186+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.527+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*936+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1072+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.825+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.249+20G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.825+20G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36485
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/2-63660860-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660860
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660860
    reference: chr 2
allele count: 6
allele frequency: 6.173220569170936e-5
allele num: 97194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.825+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.249+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.186+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*936+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.527+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.825+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.348+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1072+19T>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.249+19T>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37715
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-63660898-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660898
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660898
    reference: chr 2
allele count: 1
allele frequency: 8.333333333333334e-6
allele num: 120000
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.230A>G
  hgvsp: ENSP00000386769.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.508A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.806A>G
  hgvsp: ENSP00000387222.3:p.Tyr269Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.329A>G
  hgvsp: ENSP00000381552.3:p.Tyr110Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.230A>G
  hgvsp: ENSP00000386592.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*917A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.806A>G
  hgvsp: ENSP00000272321.7:p.Tyr269Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.167A>G
  hgvsp: ENSP00000386795.2:p.Tyr56Cys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1053A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7500
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51794
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr269Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

2-63660902-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660902
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660902
    reference: chr 2
allele count: 5709
allele frequency: 4.751639644438526e-2
allele num: 120148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.802G>A
  hgvsp: ENSP00000387222.3:p.Gly268Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.802G>A
  hgvsp: ENSP00000272321.7:p.Gly268Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1049G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.325G>A
  hgvsp: ENSP00000381552.3:p.Gly109Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.504G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.226G>A
  hgvsp: ENSP00000386769.1:p.Gly76Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.226G>A
  hgvsp: ENSP00000386592.1:p.Gly76Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.163G>A
  hgvsp: ENSP00000386795.2:p.Gly55Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*913G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 44161
  bin: 2.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 563
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 2.75e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.75e1
  variant carriers: 529
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 317
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 721
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 251
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 3.25e1
  variant carriers: 448
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 708
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.25e1
  variant carriers: 673
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 3
hgvs: p.Gly268Ser
num of homozygotes: 200
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-63660903-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660903
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660903
    reference: chr 2
allele count: 2
allele frequency: 1.6641427168794e-5
allele num: 120182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.503G>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1048G>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.801G>T
  hgvsp: ENST00000272321.7:c.801G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.324G>T
  hgvsp: ENST00000398544.3:c.324G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.801G>T
  hgvsp: ENST00000409562.3:c.801G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.162G>T
  hgvsp: ENST00000409354.2:c.162G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.225G>T
  hgvsp: ENST00000409199.1:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.225G>T
  hgvsp: ENST00000409120.1:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*912G>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51557
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu267Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-63660906-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660906
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660906
    reference: chr 2
allele count: 2
allele frequency: 1.663367654152597e-5
allele num: 120238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.321C>T
  hgvsp: ENST00000398544.3:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*909C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.798C>T
  hgvsp: ENST00000409562.3:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.798C>T
  hgvsp: ENST00000272321.7:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1045C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.159C>T
  hgvsp: ENST00000409354.2:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.500C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.222C>T
  hgvsp: ENST00000409199.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.222C>T
  hgvsp: ENST00000409120.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51578
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu266Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

2-63660917-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660917
    reference: chr 2
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.211A>C
  hgvsp: ENSP00000386592.1:p.Asn71His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.489A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.787A>C
  hgvsp: ENSP00000272321.7:p.Asn263His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1034A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.148A>C
  hgvsp: ENSP00000386795.2:p.Asn50His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.310A>C
  hgvsp: ENSP00000381552.3:p.Asn104His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*898A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.211A>C
  hgvsp: ENSP00000386769.1:p.Asn71His
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.787A>C
  hgvsp: ENSP00000387222.3:p.Asn263His
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn263His
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

2-63660917-TGGCTCTGTCCTTCTCAGAAGAAATGGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660890
    reference: chr 2
allele count: 32
allele frequency: 2.6590882651111e-4
allele num: 120342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsp: ENSP00000381552.3:p.Pro95_Ala103del
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsp: ENSP00000387222.3:p.Pro254_Ala262del
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsp: ENSP00000386795.2:p.Pro41_Ala49del
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsp: ENSP00000386769.1:p.Pro62_Ala70del
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsp: ENSP00000386592.1:p.Pro62_Ala70del
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsp: ENSP00000272321.7:p.Pro254_Ala262del
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44915
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro254_Ala262del
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: TGGCTCTGTCCTTCTCAGAAGAAATGGG
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

2-63660923-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660923
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660923
    reference: chr 2
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.142A>G
  hgvsp: ENSP00000386795.2:p.Arg48Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.483A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*892A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.205A>G
  hgvsp: ENSP00000386769.1:p.Arg69Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1028A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.781A>G
  hgvsp: ENSP00000272321.7:p.Arg261Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.304A>G
  hgvsp: ENSP00000381552.3:p.Arg102Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.205A>G
  hgvsp: ENSP00000386592.1:p.Arg69Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.781A>G
  hgvsp: ENSP00000387222.3:p.Arg261Gly
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg261Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-63660924-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660924
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660924
    reference: chr 2
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.780C>A
  hgvsp: ENSP00000272321.7:p.Asp260Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.141C>A
  hgvsp: ENSP00000386795.2:p.Asp47Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.204C>A
  hgvsp: ENSP00000386769.1:p.Asp68Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.303C>A
  hgvsp: ENSP00000381552.3:p.Asp101Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*891C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.204C>A
  hgvsp: ENSP00000386592.1:p.Asp68Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.482C>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.780C>A
  hgvsp: ENSP00000387222.3:p.Asp260Glu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1027C>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp260Glu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

2-63660933-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660933
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660933
    reference: chr 2
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.294T>A
  hgvsp: ENST00000398544.3:c.294T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.473T>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.771T>A
  hgvsp: ENST00000409562.3:c.771T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1018T>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.771T>A
  hgvsp: ENST00000272321.7:c.771T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.195T>A
  hgvsp: ENST00000409120.1:c.195T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*882T>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.195T>A
  hgvsp: ENST00000409199.1:c.195T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.132T>A
  hgvsp: ENST00000409354.2:c.132T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser257Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-63660934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660934
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660934
    reference: chr 2
allele count: 2
allele frequency: 1.661874927292972e-5
allele num: 120346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.194C>T
  hgvsp: ENSP00000386769.1:p.Ser65Phe
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.131C>T
  hgvsp: ENSP00000386795.2:p.Ser44Phe
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.194C>T
  hgvsp: ENSP00000386592.1:p.Ser65Phe
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1017C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.770C>T
  hgvsp: ENSP00000387222.3:p.Ser257Phe
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.293C>T
  hgvsp: ENSP00000381552.3:p.Ser98Phe
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.770C>T
  hgvsp: ENSP00000272321.7:p.Ser257Phe
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.472C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*881C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser257Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

2-63660935-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660935
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660935
    reference: chr 2
allele count: 1
allele frequency: 8.307579835842223e-6
allele num: 120372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.292T>C
  hgvsp: ENSP00000381552.3:p.Ser98Pro
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.769T>C
  hgvsp: ENSP00000272321.7:p.Ser257Pro
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1016T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.769T>C
  hgvsp: ENSP00000387222.3:p.Ser257Pro
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.130T>C
  hgvsp: ENSP00000386795.2:p.Ser44Pro
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.193T>C
  hgvsp: ENSP00000386592.1:p.Ser65Pro
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.193T>C
  hgvsp: ENSP00000386769.1:p.Ser65Pro
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*880T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.471T>C
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser257Pro
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

2-63660941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660941
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660941
    reference: chr 2
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*874A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.286A>G
  hgvsp: ENSP00000381552.3:p.Ile96Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.763A>G
  hgvsp: ENSP00000387222.3:p.Ile255Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.124A>G
  hgvsp: ENSP00000386795.2:p.Ile42Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1010A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.465A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.187A>G
  hgvsp: ENSP00000386769.1:p.Ile63Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.763A>G
  hgvsp: ENSP00000272321.7:p.Ile255Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.187A>G
  hgvsp: ENSP00000386592.1:p.Ile63Val
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51465
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile255Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

2-63660946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660946
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660946
    reference: chr 2
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.182C>T
  hgvsp: ENSP00000386769.1:p.Ala61Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1005C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.119C>T
  hgvsp: ENSP00000386795.2:p.Ala40Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.281C>T
  hgvsp: ENSP00000381552.3:p.Ala94Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.758C>T
  hgvsp: ENSP00000387222.3:p.Ala253Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.758C>T
  hgvsp: ENSP00000272321.7:p.Ala253Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.182C>T
  hgvsp: ENSP00000386592.1:p.Ala61Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*869C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.460C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51412
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala253Val
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: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-63660947-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660947
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660947
    reference: chr 2
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.459G>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.181G>T
  hgvsp: ENSP00000386592.1:p.Ala61Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.280G>T
  hgvsp: ENSP00000381552.3:p.Ala94Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*868G>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.757G>T
  hgvsp: ENSP00000387222.3:p.Ala253Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.1004G>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.181G>T
  hgvsp: ENSP00000386769.1:p.Ala61Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.757G>T
  hgvsp: ENSP00000272321.7:p.Ala253Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.118G>T
  hgvsp: ENSP00000386795.2:p.Ala40Ser
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala253Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

2-63660965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660965
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660965
    reference: chr 2
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.163G>A
  hgvsp: ENSP00000386769.1:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.262G>A
  hgvsp: ENSP00000381552.3:p.Asp88Asn
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.100G>A
  hgvsp: ENSP00000386795.2:p.Asp34Asn
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*850G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.739G>A
  hgvsp: ENSP00000272321.7:p.Asp247Asn
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.163G>A
  hgvsp: ENSP00000386592.1:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.441G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.986G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.739G>A
  hgvsp: ENSP00000387222.3:p.Asp247Asn
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp247Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-63660966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660966
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660966
    reference: chr 2
allele count: 9
allele frequency: 7.472848649905344e-5
allele num: 120436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.738C>T
  hgvsp: ENST00000409562.3:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*849C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.738C>T
  hgvsp: ENST00000272321.7:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.162C>T
  hgvsp: ENST00000409199.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.985C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.162C>T
  hgvsp: ENST00000409120.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.99C>T
  hgvsp: ENST00000409354.2:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.440C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.261C>T
  hgvsp: ENST00000398544.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51528
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn246Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

2-63660968-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660968
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660968
    reference: chr 2
allele count: 1
allele frequency: 8.301786544464368e-6
allele num: 120456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.160A>G
  hgvsp: ENSP00000386769.1:p.Asn54Asp
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.736A>G
  hgvsp: ENSP00000387222.3:p.Asn246Asp
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.160A>G
  hgvsp: ENSP00000386592.1:p.Asn54Asp
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.983A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.259A>G
  hgvsp: ENSP00000381552.3:p.Asn87Asp
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.438A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.97A>G
  hgvsp: ENSP00000386795.2:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.736A>G
  hgvsp: ENSP00000272321.7:p.Asn246Asp
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*847A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn246Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS

2-63660972-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660972
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660972
    reference: chr 2
allele count: 4
allele frequency: 3.321100612743063e-5
allele num: 120442
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.732G>C
  hgvsp: ENST00000272321.7:c.732G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.255G>C
  hgvsp: ENST00000398544.3:c.255G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*843G>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.156G>C
  hgvsp: ENST00000409120.1:c.156G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.732G>C
  hgvsp: ENST00000409562.3:c.732G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.93G>C
  hgvsp: ENST00000409354.2:c.93G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.156G>C
  hgvsp: ENST00000409199.1:c.156G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.434G>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.979G>C
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu244Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

2-63660976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660976
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660976
    reference: chr 2
allele count: 4
allele frequency: 3.320383836371484e-5
allele num: 120468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.251C>T
  hgvsp: ENSP00000381552.3:p.Pro84Leu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*839C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.975C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.152C>T
  hgvsp: ENSP00000386769.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.89C>T
  hgvsp: ENSP00000386795.2:p.Pro30Leu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.152C>T
  hgvsp: ENSP00000386592.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.728C>T
  hgvsp: ENSP00000387222.3:p.Pro243Leu
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.430C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.728C>T
  hgvsp: ENSP00000272321.7:p.Pro243Leu
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro243Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

2-63660977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660977
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660977
    reference: chr 2
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.151C>T
  hgvsp: ENSP00000386592.1:p.Pro51Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.250C>T
  hgvsp: ENSP00000381552.3:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.88C>T
  hgvsp: ENSP00000386795.2:p.Pro30Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.151C>T
  hgvsp: ENSP00000386769.1:p.Pro51Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.429C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.974C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.727C>T
  hgvsp: ENSP00000387222.3:p.Pro243Ser
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*838C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.727C>T
  hgvsp: ENSP00000272321.7:p.Pro243Ser
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51783
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro243Ser
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

2-63660990-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660990
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660990
    reference: chr 2
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.961T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.75T>C
  hgvsp: ENST00000409354.2:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.237T>C
  hgvsp: ENST00000398544.3:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.138T>C
  hgvsp: ENST00000409199.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.138T>C
  hgvsp: ENST00000409120.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.714T>C
  hgvsp: ENST00000272321.7:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*825T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.714T>C
  hgvsp: ENST00000409562.3:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.416T>C
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val238Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

2-63660996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63660996
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63660996
    reference: chr 2
allele count: 3
allele frequency: 2.489750526997195e-5
allele num: 120494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.231T>C
  hgvsp: ENST00000398544.3:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.955T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.132T>C
  hgvsp: ENST00000409120.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.708T>C
  hgvsp: ENST00000409562.3:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*819T>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.132T>C
  hgvsp: ENST00000409199.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.69T>C
  hgvsp: ENST00000409354.2:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.708T>C
  hgvsp: ENST00000272321.7:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.410T>C
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp236Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

2-63661001-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661001
    reference: chr 2
allele count: 1
allele frequency: 8.300132802124834e-6
allele num: 120480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*814C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.127C>T
  hgvsp: ENSP00000386769.1:p.His43Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.703C>T
  hgvsp: ENSP00000387222.3:p.His235Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.703C>T
  hgvsp: ENSP00000272321.7:p.His235Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.950C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.226C>T
  hgvsp: ENSP00000381552.3:p.His76Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.127C>T
  hgvsp: ENSP00000386592.1:p.His43Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.64C>T
  hgvsp: ENSP00000386795.2:p.His22Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.405C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His235Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

2-63661006-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661006
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661006
    reference: chr 2
allele count: 1
allele frequency: 8.30137304710199e-6
allele num: 120462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.122G>A
  hgvsp: ENSP00000386592.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.122G>A
  hgvsp: ENSP00000386769.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.221G>A
  hgvsp: ENSP00000381552.3:p.Cys74Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.945G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.698G>A
  hgvsp: ENSP00000272321.7:p.Cys233Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.698G>A
  hgvsp: ENSP00000387222.3:p.Cys233Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.59G>A
  hgvsp: ENSP00000386795.2:p.Cys20Tyr
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.400G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*809G>A
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys233Tyr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

2-63661008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661008
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661008
    reference: chr 2
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.120C>T
  hgvsp: ENST00000409199.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*807C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.219C>T
  hgvsp: ENST00000398544.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.696C>T
  hgvsp: ENST00000272321.7:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.398C>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.57C>T
  hgvsp: ENST00000409354.2:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.696C>T
  hgvsp: ENST00000409562.3:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.120C>T
  hgvsp: ENST00000409120.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.943C>T
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn232Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-63661013-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661013
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661013
    reference: chr 2
allele count: 8
allele frequency: 6.642863073984888e-5
allele num: 120430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.115A>G
  hgvsp: ENSP00000386769.1:p.Ile39Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.938A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.115A>G
  hgvsp: ENSP00000386592.1:p.Ile39Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.52A>G
  hgvsp: ENSP00000386795.2:p.Ile18Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.214A>G
  hgvsp: ENSP00000381552.3:p.Ile72Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*802A>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.691A>G
  hgvsp: ENSP00000272321.7:p.Ile231Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.691A>G
  hgvsp: ENSP00000387222.3:p.Ile231Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.393A>G
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile231Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

2-63661015-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661015
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661015
    reference: chr 2
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*800C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.50C>G
  hgvsp: ENSP00000386795.2:p.Ala17Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.391C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.113C>G
  hgvsp: ENSP00000386592.1:p.Ala38Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.689C>G
  hgvsp: ENSP00000272321.7:p.Ala230Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.689C>G
  hgvsp: ENSP00000387222.3:p.Ala230Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.113C>G
  hgvsp: ENSP00000386769.1:p.Ala38Gly
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.936C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.212C>G
  hgvsp: ENSP00000381552.3:p.Ala71Gly
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala230Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

2-63661019-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661019
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661019
    reference: chr 2
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.208C>G
  hgvsp: ENSP00000381552.3:p.Leu70Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.932C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.109C>G
  hgvsp: ENSP00000386769.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.685C>G
  hgvsp: ENSP00000272321.7:p.Leu229Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.387C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.685C>G
  hgvsp: ENSP00000387222.3:p.Leu229Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*796C>G
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.109C>G
  hgvsp: ENSP00000386592.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.46C>G
  hgvsp: ENSP00000386795.2:p.Leu16Val
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu229Val
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

2-63661024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661024
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661024
    reference: chr 2
allele count: 3
allele frequency: 2.492812390939458e-5
allele num: 120346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.104G>A
  hgvsp: ENSP00000386769.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.41G>A
  hgvsp: ENSP00000386795.2:p.Arg14Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.680G>A
  hgvsp: ENSP00000272321.7:p.Arg227Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.927G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*791G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.203G>A
  hgvsp: ENSP00000381552.3:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.382G>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.104G>A
  hgvsp: ENSP00000386592.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.680G>A
  hgvsp: ENSP00000387222.3:p.Arg227Gln
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg227Gln
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: C
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

2-63661027-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661027
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661027
    reference: chr 2
allele count: 1
allele frequency: 8.313104778372627e-6
allele num: 120292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.200A>T
  hgvsp: ENSP00000381552.3:p.Glu67Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.677A>T
  hgvsp: ENSP00000272321.7:p.Glu226Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.677A>T
  hgvsp: ENSP00000387222.3:p.Glu226Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.101A>T
  hgvsp: ENSP00000386769.1:p.Glu34Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.924A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.101A>T
  hgvsp: ENSP00000386592.1:p.Glu34Val
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*788A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.379A>T
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.38A>T
  hgvsp: ENSP00000386795.2:p.Glu13Val
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu226Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

2-63661032-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661032
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661032
    reference: chr 2
allele count: 1
allele frequency: 8.3166999334664e-6
allele num: 120240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.96A>C
  hgvsp: ENST00000409120.1:c.96A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.919A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.672A>C
  hgvsp: ENST00000272321.7:c.672A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*783A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.33A>C
  hgvsp: ENST00000409354.2:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.96A>C
  hgvsp: ENST00000409199.1:c.96A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.374A>C
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.672A>C
  hgvsp: ENST00000409562.3:c.672A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.195A>C
  hgvsp: ENST00000398544.3:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr224Thr
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: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

2-63661042-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63661042
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 63661042
    reference: chr 2
allele count: 1
allele frequency: 8.350312301680083e-6
allele num: 119756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386769
  ensembl transcript: ENST00000409120
  gene symbol: WDPCP
  hgvsc: ENST00000409120.1:c.86T>A
  hgvsp: ENSP00000386769.1:p.Ile29Lys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000493315
  gene symbol: WDPCP
  hgvsc: ENST00000493315.1:n.364T>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143951
  ensembl transcript: ENST00000409835
  gene symbol: WDPCP
  hgvsc: ENST00000409835.1:n.909T>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386795
  ensembl transcript: ENST00000409354
  gene symbol: WDPCP
  hgvsc: ENST00000409354.2:c.23T>A
  hgvsp: ENSP00000386795.2:p.Ile8Lys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000381552
  ensembl transcript: ENST00000398544
  gene symbol: WDPCP
  hgvsc: ENST00000398544.3:c.185T>A
  hgvsp: ENSP00000381552.3:p.Ile62Lys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000411429
  ensembl transcript: ENST00000417238
  gene symbol: WDPCP
  hgvsc: ENST00000417238.1:c.*773T>A
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000387222
  ensembl transcript: ENST00000409562
  gene symbol: WDPCP
  hgvsc: ENST00000409562.3:c.662T>A
  hgvsp: ENSP00000387222.3:p.Ile221Lys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000272321
  ensembl transcript: ENST00000272321
  gene symbol: WDPCP
  hgvsc: ENST00000272321.7:c.662T>A
  hgvsp: ENSP00000272321.7:p.Ile221Lys
  variant of: http://identifiers.org/hgnc/28027
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143951
  ensembl protein: ENSP00000386592
  ensembl transcript: ENST00000409199
  gene symbol: WDPCP
  hgvsc: ENST00000409199.1:c.86T>A
  hgvsp: ENSP00000386592.1:p.Ile29Lys
  variant of: http://identifiers.org/hgnc/28027
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile221Lys
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 3207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6003
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.491620111731844e-4
allele num: 8592
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

FS
type: SiteQuality
SIO_000300: 7.284e0

DP
type: SiteQuality
SIO_000300: 1.689657e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.29e-1

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6004
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31148
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.697e1

DP
type: SiteQuality
SIO_000300: 1.689939e6

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.97e-1

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7810
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31138
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 71
allele frequency: 4.313487241798299e-3
allele num: 16460
num of homozygotes: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.692648e6

QD
type: SiteQuality
SIO_000300: 1.62e1

FS
type: SiteQuality
SIO_000300: 1.094e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.79e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6029
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.434e0

DP
type: SiteQuality
SIO_000300: 1.691951e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 4.218e0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.413e1

MQ
type: SiteQuality
SIO_000300: 6.005e1

GenotypeQuality
all individuals: 3309
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3219
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7820
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6029
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001741009785676e-5
allele num: 66628
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: 11528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

DP
type: SiteQuality
SIO_000300: 1.692754e6

FS
type: SiteQuality
SIO_000300: 3.073e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

GenotypeQuality
all individuals: 4423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.494060097833683e-4
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.032e0

FS
type: SiteQuality
SIO_000300: 1.2461e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: -8.673999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

DP
type: SiteQuality
SIO_000300: 1.693913e6

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6033
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.276e1

DP
type: SiteQuality
SIO_000300: 1.693784e6

FS
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.946e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6059
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 7.25e1
variant carriers: 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: 16498
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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

DP
type: SiteQuality
SIO_000300: 1.701147e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.645e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.97e-1

QD
type: SiteQuality
SIO_000300: 7.65e0

FS
type: SiteQuality
SIO_000300: 4.876e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.483e1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

DP
type: SiteQuality
SIO_000300: 1.70101e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

GenotypeQuality
all individuals: 31358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 58
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 8005
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16333178222429e-4
allele num: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
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: 16498
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.928e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.701339e6

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

VQSLOD
type: SiteQuality
SIO_000300: -1.111e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 15
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 43

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.501907422426482e-4
allele num: 66582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

South Asian
type: Population
allele count: 33
allele frequency: 1.999757605138771e-3
allele num: 16502
num of homozygotes: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.703121e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

QD
type: SiteQuality
SIO_000300: 1.167e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1732
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.700672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.584e-1

FS
type: SiteQuality
SIO_000300: 2.441e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

QD
type: SiteQuality
SIO_000300: 1.526e1

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8008
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1731
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503985561738607e-5
allele num: 66490
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.18e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

QD
type: SiteQuality
SIO_000300: 1.125e1

FS
type: SiteQuality
SIO_000300: 1.757e0

DP
type: SiteQuality
SIO_000300: 1.699782e6

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

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

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31126
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

DP
type: SiteQuality
SIO_000300: 1.698974e6

FS
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.337e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 5
allele frequency: 5.830223880597014e-4
allele num: 8576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
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: 66328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.034340091021928e-4
allele num: 9668
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 1.69645e6

QD
type: SiteQuality
SIO_000300: 1.155e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
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: 11508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.212e1

DP
type: SiteQuality
SIO_000300: 1.695903e6

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 2.347e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.423948612289419e-4
allele num: 16502
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

VQSLOD
type: SiteQuality
SIO_000300: -2.254e0

FS
type: SiteQuality
SIO_000300: 1.6585e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

DP
type: SiteQuality
SIO_000300: 1.693352e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.5e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516944267467613e-5
allele num: 65922
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
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: 8566
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.91e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

DP
type: SiteQuality
SIO_000300: 1.687253e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.414e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.946e0

QD
type: SiteQuality
SIO_000300: 9.09e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.057529610829103e-4
allele num: 9456
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: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65790
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.398e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 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: 8550
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.374788494077834e-3
allele num: 9456
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: 65790
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.247e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.684051e6

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.03e-1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.398e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

African
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allele count: 6
allele frequency: 6.361323155216285e-4
allele num: 9432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

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

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

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

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65674
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9426
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.343017806935333e-4
allele num: 8536
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.11e-1

DP
type: SiteQuality
SIO_000300: 1.680213e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 7.999e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.429e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.051571559353067e-5
allele num: 65540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.677172e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.236e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52592547379986e-5
allele num: 65534
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

MQ
type: SiteQuality
SIO_000300: 5.91e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.676599e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

FS
type: SiteQuality
SIO_000300: 4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.051850947599719e-5
allele num: 65534
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.676599e6

QD
type: SiteQuality
SIO_000300: 1.278e1

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

FS
type: SiteQuality
SIO_000300: 4.99e-1

MQ
type: SiteQuality
SIO_000300: 5.91e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
all individuals: 7855
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9326
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.838e0

QD
type: SiteQuality
SIO_000300: 1.515e1

MQ
type: SiteQuality
SIO_000300: 5.916e1

VQSLOD
type: SiteQuality
SIO_000300: -1.794e0

FS
type: SiteQuality
SIO_000300: 8.539e0

DP
type: SiteQuality
SIO_000300: 1.672632e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.752e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 23

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9332
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

East Asian
type: Population
allele count: 22
allele frequency: 2.582765907490021e-3
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65398
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.14e-1

DP
type: SiteQuality
SIO_000300: 1.673504e6

QD
type: SiteQuality
SIO_000300: 1.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.817e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21300339640951e-4
allele num: 16488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65222
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.801e1

VQSLOD
type: SiteQuality
SIO_000300: -1.762e0

FS
type: SiteQuality
SIO_000300: 5.307e0

DP
type: SiteQuality
SIO_000300: 1.669435e6

MQRankSum
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 85

GenotypeQuality
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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: 27

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 77

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 20420

GenotypeQuality
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variant carriers: 47

GenotypeQuality
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bin: 6.25e1
variant carriers: 60

Latino
type: Population
allele count: 1885
allele frequency: 1.649168853893263e-1
allele num: 11430
num of homozygotes: 168

South Asian
type: Population
allele count: 4219
allele frequency: 2.559762164785827e-1
allele num: 16482
num of homozygotes: 601

East Asian
type: Population
allele count: 1153
allele frequency: 1.362240075614367e-1
allele num: 8464
num of homozygotes: 94

African
type: Population
allele count: 1942
allele frequency: 2.094929881337648e-1
allele num: 9270
num of homozygotes: 200

European (Non-Finnish)
type: Population
allele count: 13266
allele frequency: 2.034787410270569e-1
allele num: 65196
num of homozygotes: 1457

European (Finnish)
type: Population
allele count: 848
allele frequency: 1.285237950894211e-1
allele num: 6598
num of homozygotes: 55

Other
type: Population
allele count: 190
allele frequency: 2.130044843049327e-1
allele num: 892
num of homozygotes: 23

QD
type: SiteQuality
SIO_000300: 1.554e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.177e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.39e-2

DP
type: SiteQuality
SIO_000300: 2.277773e6

FS
type: SiteQuality
SIO_000300: 8.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 335
bin: 4.75e1
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GenotypeQuality
all individuals: 4326
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180080245456691e-4
allele num: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537846399901578e-5
allele num: 65026
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.026004e6

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.503e1

FS
type: SiteQuality
SIO_000300: 4.016e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

GenotypeQuality
all individuals: 19317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.63e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.11e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.021231e6

FS
type: SiteQuality
SIO_000300: 7.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

GenotypeQuality
all individuals: 1715
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2840
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19275
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14265
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4319
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 7.648601398601399e-4
allele num: 9152
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.751313485113835e-4
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64774
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.145e0

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

FS
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.291e1

DP
type: SiteQuality
SIO_000300: 2.02072e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

GenotypeQuality
all individuals: 365
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4319
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14265
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64774
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.145e0

FS
type: SiteQuality
SIO_000300: 2.06e0

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.02072e6

QD
type: SiteQuality
SIO_000300: 1.291e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

GenotypeQuality
all individuals: 4529
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5592
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.056766762649116e-4
allele num: 4862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.44889e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 6.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.977e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

GenotypeQuality
all individuals: 162
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 7
allele frequency: 5.767963085036256e-4
allele num: 12136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8026
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.14e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 9.30383e5

GenotypeQuality
all individuals: 1221
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 20506
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3720
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.249063202598052e-4
allele num: 40030
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.69933e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

QD
type: SiteQuality
SIO_000300: 1.716e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.191e0

VQSLOD
type: SiteQuality
SIO_000300: -5.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12142
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.887873721861514e-5
allele num: 51442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13922
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.433e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.178399e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.866e-1

GenotypeQuality
all individuals: 1001
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38595
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11178
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2560
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.326259946949602e-3
allele num: 754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.481548905829257e-5
allele num: 52734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 1.196244e6

VQSLOD
type: SiteQuality
SIO_000300: 4.81e-1

QD
type: SiteQuality
SIO_000300: 1.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1020
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66332
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.022704029453876e-4
allele num: 9778
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: -1.432e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.217e0

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.396682e6

QD
type: SiteQuality
SIO_000300: 7.94e0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 14

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 730
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47696
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 836
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 6560
bin: 9.75e1
variant carriers: 5440

GenotypeQuality
all individuals: 252
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2834
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 11

European (Non-Finnish)
type: Population
allele count: 4353
allele frequency: 6.55315689639599e-2
allele num: 66426
num of homozygotes: 148

East Asian
type: Population
allele count: 2
allele frequency: 2.331545814875262e-4
allele num: 8578
num of homozygotes: 0

South Asian
type: Population
allele count: 338
allele frequency: 2.052714684805053e-2
allele num: 16466
num of homozygotes: 9

European (Finnish)
type: Population
allele count: 740
allele frequency: 1.126674786845311e-1
allele num: 6568
num of homozygotes: 38

African
type: Population
allele count: 96
allele frequency: 9.809932556713672e-3
allele num: 9786
num of homozygotes: 1

Other
type: Population
allele count: 47
allele frequency: 5.245535714285714e-2
allele num: 896
num of homozygotes: 4

Latino
type: Population
allele count: 133
allele frequency: 1.16380819040952e-2
allele num: 11428
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.25e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

FS
type: SiteQuality
SIO_000300: 1.418e0

DP
type: SiteQuality
SIO_000300: 1.567906e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

QD
type: SiteQuality
SIO_000300: 1.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.331545814875262e-4
allele num: 8578
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.430424e6

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.576e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.119e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e0

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3618
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504483360414034e-5
allele num: 66468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.431143e6

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

QD
type: SiteQuality
SIO_000300: 1.067e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

FS
type: SiteQuality
SIO_000300: 1.792e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.263e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

GenotypeQuality
all individuals: 51584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66534
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: -2.928e0

FS
type: SiteQuality
SIO_000300: 1.9785e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.487e0

MQ
type: SiteQuality
SIO_000300: 5.344e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 1.433628e6

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 9.75e1
variant carriers: 32

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
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: 11454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 4.659271951182854e-4
allele num: 66534
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.9785e1

VQSLOD
type: SiteQuality
SIO_000300: -2.928e0

DP
type: SiteQuality
SIO_000300: 1.433628e6

MQ
type: SiteQuality
SIO_000300: 5.344e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: -4.487e0

QD
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3639
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51568
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.8395e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 1.433101e6

QD
type: SiteQuality
SIO_000300: 1.317e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.692e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-1

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

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51532
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.497e0

FS
type: SiteQuality
SIO_000300: 2.3541e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.299e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

DP
type: SiteQuality
SIO_000300: 1.432896e6

VQSLOD
type: SiteQuality
SIO_000300: -4.576e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.4e-1

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

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

DP
type: SiteQuality
SIO_000300: 1.433608e6

VQSLOD
type: SiteQuality
SIO_000300: -3.341e0

FS
type: SiteQuality
SIO_000300: 2.1836e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.06e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.421e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 8.791e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.972e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.433871e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.918e1

FS
type: SiteQuality
SIO_000300: 1.9064e1

QD
type: SiteQuality
SIO_000300: 1.066e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.27e-1

DP
type: SiteQuality
SIO_000300: 1.43356e6

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

African
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allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

DP
type: SiteQuality
SIO_000300: 1.434134e6

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.45e0

FS
type: SiteQuality
SIO_000300: 1.7447e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.002e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 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: 9790
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.639e0

QD
type: SiteQuality
SIO_000300: 1.311e1

FS
type: SiteQuality
SIO_000300: 3.906e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.271e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: -1.95e-1

DP
type: SiteQuality
SIO_000300: 1.435213e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.02e0

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

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

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

East 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
allele num: 900
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.506263706552107e-5
allele num: 66574
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Other
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South Asian
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East Asian
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allele frequency: 3.48594004183128e-4
allele num: 8606
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African
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allele frequency: 2.042483660130719e-4
allele num: 9792
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
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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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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: 6594
num of homozygotes: 0

South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66586
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East Asian
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Other
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Latino
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allele frequency: 0.0e0
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African
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.374e0

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

DP
type: SiteQuality
SIO_000300: 1.437197e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.469e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 1.4319e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.424536307431204e-4
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

DP
type: SiteQuality
SIO_000300: 1.438274e6

FS
type: SiteQuality
SIO_000300: 1.628e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.304e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.09e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 4.084967320261438e-4
allele num: 9792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.633e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.438654e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.51e-1

QD
type: SiteQuality
SIO_000300: 2.015e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

DP
type: SiteQuality
SIO_000300: 1.438603e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.661e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

DP
type: SiteQuality
SIO_000300: 1.439422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.558e0

FS
type: SiteQuality
SIO_000300: 2.1193e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.298e0

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

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

African
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allele count: 3
allele frequency: 3.06309985705534e-4
allele num: 9794
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.452e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.439648e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

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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bin: 9.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

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

East Asian
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South Asian
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allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Latino
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BaseQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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VQSLOD
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MQ
type: SiteQuality
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MQRankSum
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.230125523012552e-4
allele num: 11472
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 4.151e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

MQRankSum
type: SiteQuality
SIO_000300: 3.76e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.439453e6

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 2.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3603
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.439079e6

QD
type: SiteQuality
SIO_000300: 1.548e1

FS
type: SiteQuality
SIO_000300: 4.915e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516070345664039e-4
allele num: 6596
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 9.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.382e0

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.52e-1

DP
type: SiteQuality
SIO_000300: 1.438992e6

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 7.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508972855983407e-5
allele num: 66534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.26e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 1.085e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.21e-1

DP
type: SiteQuality
SIO_000300: 1.43854e6

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 51782
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 866
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.736676568233443e-5
allele num: 11446
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.437708e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.477e0

FS
type: SiteQuality
SIO_000300: 9.81e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

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

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.557e0

VQSLOD
type: SiteQuality
SIO_000300: 2.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.799e0

DP
type: SiteQuality
SIO_000300: 1.437062e6

QD
type: SiteQuality
SIO_000300: 1.257e1

MQRankSum
type: SiteQuality
SIO_000300: -1.284e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0