19-32954250-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954250
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954250
    reference: chr 19
allele count: 1
allele frequency: 8.601558602418759e-6
allele num: 116258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.107-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1323-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.236-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.622-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1323-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1323-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.42-22T>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.860-22T>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

19-32954250-T-TGTATGTTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954250
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954259
    reference: chr 19
allele count: 4
allele frequency: 3.440623440967504e-5
allele num: 116258
alternate allele: TGTATGTTGC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29765
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11349
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6625
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7618
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

19-32954252-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954252
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954252
    reference: chr 19
allele count: 6
allele frequency: 5.127942156812471e-5
allele num: 117006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1323-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.236-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.42-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.107-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1323-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.622-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1323-20T>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.860-20T>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30180
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7650
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

19-32954252-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954252
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954252
    reference: chr 19
allele count: 1
allele frequency: 8.546570261354118e-6
allele num: 117006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1323-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.107-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.42-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1323-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.860-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.622-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1323-20T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.236-20T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

19-32954254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954254
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954254
    reference: chr 19
allele count: 1
allele frequency: 8.506873553831496e-6
allele num: 117552
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.236-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.622-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.42-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1323-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.107-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1323-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1323-18T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.860-18T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3429
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

19-32954267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954267
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954267
    reference: chr 19
allele count: 1
allele frequency: 8.325701440346349e-6
allele num: 120110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.236-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.107-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1323-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.860-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.42-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1323-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.622-5C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1323-5C>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2761
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1323-5C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

19-32954287-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954287
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954287
    reference: chr 19
allele count: 3
allele frequency: 2.478069088566189e-5
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.875A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1338A>G
  hgvsp: ENST00000586987.1:c.1338A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1338A>G
  hgvsp: ENST00000342179.5:c.1338A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.251A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.122A>G
  hgvsp: ENST00000592832.2:c.122A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.57A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1338A>G
  hgvsp: ENST00000392250.2:c.1338A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.637A>G
  hgvsp: ENST00000588648.3:c.637A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32782
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln446Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD

19-32954290-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954290
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954290
    reference: chr 19
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1341A>G
  hgvsp: ENST00000392250.2:c.1341A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.125A>G
  hgvsp: ENST00000592832.2:c.125A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.878A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1341A>G
  hgvsp: ENST00000342179.5:c.1341A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.640A>G
  hgvsp: ENST00000588648.3:c.640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1341A>G
  hgvsp: ENST00000586987.1:c.1341A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.60A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.254A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln447Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

19-32954291-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954291
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954291
    reference: chr 19
allele count: 2
allele frequency: 1.651473114017704e-5
allele num: 121104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1342T>C
  hgvsp: ENSP00000376081.2:p.Ser448Pro
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1342T>C
  hgvsp: ENSP00000466086.1:p.Ser448Pro
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1342T>C
  hgvsp: ENSP00000344937.4:p.Ser448Pro
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.255T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.126T>C
  hgvsp: ENSP00000474174.1:p.Ser43Pro
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.879T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.61T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.641T>C
  hgvsp: ENSP00000465997.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser448Pro
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

19-32954293-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954293
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954293
    reference: chr 19
allele count: 10
allele frequency: 8.256820133430213e-5
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1344C>T
  hgvsp: ENST00000586987.1:c.1344C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1344C>T
  hgvsp: ENST00000392250.2:c.1344C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.63C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.881C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.128C>T
  hgvsp: ENST00000592832.2:c.128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.643C>T
  hgvsp: ENST00000588648.3:c.643C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1344C>T
  hgvsp: ENST00000342179.5:c.1344C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.257C>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser448Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

19-32954294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954294
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954294
    reference: chr 19
allele count: 20
allele frequency: 1.650873311982039e-4
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1345G>A
  hgvsp: ENSP00000344937.4:p.Val449Met
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.129G>A
  hgvsp: ENSP00000474174.1:p.Val44Met
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1345G>A
  hgvsp: ENSP00000376081.2:p.Val449Met
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.644G>A
  hgvsp: ENSP00000465997.1:p.Val216Met
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1345G>A
  hgvsp: ENSP00000466086.1:p.Val449Met
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000585597
  gene symbol: DPY19L3
  hgvsc: ENST00000585597.1:n.882G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.64G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.258G>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31962
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32785
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val449Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

19-32954302-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954302
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954302
    reference: chr 19
allele count: 55
allele frequency: 4.536830817454425e-4
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.266A>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1353A>T
  hgvsp: ENSP00000344937.4:p.Lys451Asn
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1353A>T
  hgvsp: ENSP00000376081.2:p.Lys451Asn
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.652A>T
  hgvsp: ENSP00000465997.1:p.Lys218Asn
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.137A>T
  hgvsp: ENSP00000474174.1:p.Lys46Asn
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1353A>T
  hgvsp: ENSP00000466086.1:p.Lys451Asn
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.72A>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7919
  bin: 9.75e1
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys451Asn
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

19-32954313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954313
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954313
    reference: chr 19
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1364G>A
  hgvsp: ENSP00000466086.1:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1364G>A
  hgvsp: ENSP00000376081.2:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.277G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1364G>A
  hgvsp: ENSP00000344937.4:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.663G>A
  hgvsp: ENSP00000465997.1:p.Gly222Asp
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.148G>A
  hgvsp: ENSP00000474174.1:p.Gly50Asp
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.83G>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly455Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-32954313-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954313
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954313
    reference: chr 19
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1364G>C
  hgvsp: ENSP00000466086.1:p.Gly455Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.83G>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1364G>C
  hgvsp: ENSP00000376081.2:p.Gly455Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.663G>C
  hgvsp: ENSP00000465997.1:p.Gly222Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.277G>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1364G>C
  hgvsp: ENSP00000344937.4:p.Gly455Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.148G>C
  hgvsp: ENSP00000474174.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3841
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly455Ala
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

19-32954315-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954315
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954315
    reference: chr 19
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1366A>G
  hgvsp: ENSP00000344937.4:p.Thr456Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1366A>G
  hgvsp: ENSP00000376081.2:p.Thr456Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1366A>G
  hgvsp: ENSP00000466086.1:p.Thr456Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.665A>G
  hgvsp: ENSP00000465997.1:p.Thr223Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.85A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.150A>G
  hgvsp: ENSP00000474174.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.279A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2805
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32770
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr456Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-32954316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954316
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954316
    reference: chr 19
allele count: 9
allele frequency: 7.418397626112759e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1367C>T
  hgvsp: ENSP00000376081.2:p.Thr456Ile
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.666C>T
  hgvsp: ENSP00000465997.1:p.Thr223Ile
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1367C>T
  hgvsp: ENSP00000466086.1:p.Thr456Ile
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.86C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1367C>T
  hgvsp: ENSP00000344937.4:p.Thr456Ile
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.151C>T
  hgvsp: ENSP00000474174.1:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.280C>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31850
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3838
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr456Ile
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-32954319-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954319
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954319
    reference: chr 19
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.669T>C
  hgvsp: ENSP00000465997.1:p.Val224Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.154T>C
  hgvsp: ENSP00000474174.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1370T>C
  hgvsp: ENSP00000466086.1:p.Val457Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.283T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1370T>C
  hgvsp: ENSP00000344937.4:p.Val457Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1370T>C
  hgvsp: ENSP00000376081.2:p.Val457Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.89T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7931
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7411
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val457Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

19-32954329-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954329
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954329
    reference: chr 19
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.679A>G
  hgvsp: ENST00000588648.3:c.679A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1380A>G
  hgvsp: ENST00000586987.1:c.1380A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1380A>G
  hgvsp: ENST00000392250.2:c.1380A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.164A>G
  hgvsp: ENST00000592832.2:c.164A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.99A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1380A>G
  hgvsp: ENST00000342179.5:c.1380A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.293A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7932
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys460Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

19-32954336-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954336
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954336
    reference: chr 19
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1387A>G
  hgvsp: ENSP00000376081.2:p.Thr463Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.171A>G
  hgvsp: ENSP00000474174.1:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.686A>G
  hgvsp: ENSP00000465997.1:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1387A>G
  hgvsp: ENSP00000466086.1:p.Thr463Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.300A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1387A>G
  hgvsp: ENSP00000344937.4:p.Thr463Ala
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.106A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2807
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr463Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

19-32954343-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954343
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954343
    reference: chr 19
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1394A>G
  hgvsp: ENSP00000376081.2:p.Tyr465Cys
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1394A>G
  hgvsp: ENSP00000466086.1:p.Tyr465Cys
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.693A>G
  hgvsp: ENSP00000465997.1:p.Tyr232Cys
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1394A>G
  hgvsp: ENSP00000344937.4:p.Tyr465Cys
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.307A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.178A>G
  hgvsp: ENSP00000474174.1:p.Tyr60Cys
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.113A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32802
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr465Cys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-32954350-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954350
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954350
    reference: chr 19
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1401A>G
  hgvsp: ENST00000392250.2:c.1401A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1401A>G
  hgvsp: ENST00000586987.1:c.1401A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.120A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1401A>G
  hgvsp: ENST00000342179.5:c.1401A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.700A>G
  hgvsp: ENST00000588648.3:c.700A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.314A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.185A>G
  hgvsp: ENST00000592832.2:c.185A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7934
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32813
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu467Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

19-32954359-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954359
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954359
    reference: chr 19
allele count: 16
allele frequency: 1.318239491159556e-4
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.709C>G
  hgvsp: ENST00000588648.3:c.709C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.194C>G
  hgvsp: ENST00000592832.2:c.194C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.129C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1410C>G
  hgvsp: ENST00000586987.1:c.1410C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.323C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1410C>G
  hgvsp: ENST00000392250.2:c.1410C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1410C>G
  hgvsp: ENST00000342179.5:c.1410C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32806
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr470Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

19-32954386-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954386
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954386
    reference: chr 19
allele count: 29
allele frequency: 2.389387822361374e-4
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1437T>C
  hgvsp: ENST00000392250.2:c.1437T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1437T>C
  hgvsp: ENST00000586987.1:c.1437T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.736T>C
  hgvsp: ENST00000588648.3:c.736T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1437T>C
  hgvsp: ENST00000342179.5:c.1437T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.156T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.221T>C
  hgvsp: ENST00000592832.2:c.221T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.350T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2805
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3832
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7968
  bin: 9.75e1
  variant carriers: 29
hgvs: p.Ser479Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-32954411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954411
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954411
    reference: chr 19
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+17T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+17T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+17T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+17T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+17T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+17T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+17T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32396
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7319
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-32954415-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954415
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954415
    reference: chr 19
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+21T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+21T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+21T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+21T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+21T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+21T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+21T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7961
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2793
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

19-32954416-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954416
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954415
    reference: chr 19
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+25delT
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+25delT
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+25delT
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+25delT
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+25delT
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+25delT
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+25delT
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2793
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32230
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: GT
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

19-32954420-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954420
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954420
    reference: chr 19
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+26A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+26A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+26A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+26A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+26A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+26A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+26A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3796
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-32954436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954436
    reference: chr 19
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+42C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+42C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+42C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+42C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+42C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+42C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+42C>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

19-32954437-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954437
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954437
    reference: chr 19
allele count: 1
allele frequency: 8.263506701703935e-6
allele num: 121014
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+43T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+43T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+43T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+43T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+43T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+43T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+43T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6747
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

19-32954442-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954442
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954442
    reference: chr 19
allele count: 3
allele frequency: 2.481430627471092e-5
allele num: 120898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+48A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+48A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+48A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+48A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+48A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+48A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+48A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

19-32954445-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954445
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954445
    reference: chr 19
allele count: 1
allele frequency: 8.279379377721846e-6
allele num: 120782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.358+51T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.229+51T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.164+51T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1445+51T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.744+51T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1445+51T>C
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1445+51T>C
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

19-32954725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954725
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954725
    reference: chr 19
allele count: 70830
allele frequency: 5.845409830653946e-1
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-50G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-50G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-50G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-50G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-50G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-50G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-50G>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.25e1
  variant carriers: 572
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 388
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.75e1
  variant carriers: 919
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 4.25e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 8.75e1
  variant carriers: 1919
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.75e1
  variant carriers: 468
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 2.75e1
  variant carriers: 1145
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 319
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 3.25e1
  variant carriers: 777
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 1237
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.25e1
  variant carriers: 1266
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.25e1
  variant carriers: 957
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 765
genotype depth: GenotypeDepth
  all individuals: 34076
  bin: 9.75e1
  variant carriers: 33731
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 5.25e1
  variant carriers: 407
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 8.25e1
  variant carriers: 1537
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 2393
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 3.75e1
  variant carriers: 453
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 104
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.75e1
  variant carriers: 122
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 6.75e1
  variant carriers: 240
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.25e1
  variant carriers: 166
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 52
num of homozygotes: 21227
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/19-32954734-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954734
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954734
    reference: chr 19
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-41C>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-41C>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-41C>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-41C>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-41C>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-41C>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-41C>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18251
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4346
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-32954736-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954736
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954736
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-39A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-39A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-39A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-39A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-39A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-39A>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-39A>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

19-32954737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954737
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954737
    reference: chr 19
allele count: 216
allele frequency: 1.782060590060062e-3
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-38C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-38C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-38C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-38C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-38C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-38C>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-38C>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 9.75e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13575
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18264
  bin: 9.75e1
  variant carriers: 215
genotype quality: GenotypeQuality
  all individuals: 4349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15957
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

19-32954746-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954746
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954746
    reference: chr 19
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-29C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-29C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-29C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-29C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-29C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-29C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-29C>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5014
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18151
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-32954748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954748
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954748
    reference: chr 19
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-27G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-27G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-27G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-27G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-27G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-27G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-27G>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18151
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5014
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

19-32954753-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954753
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954752
    reference: chr 19
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-21delC
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-21delC
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-21delC
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-21delC
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-21delC
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-21delC
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-21delC
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10232
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: GC
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-32954755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954755
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954755
    reference: chr 19
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-20G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-20G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-20G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-20G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-20G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-20G>A
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-20G>A
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16671
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

19-32954757-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954757
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954757
    reference: chr 19
allele count: 39
allele frequency: 3.214427007780562e-4
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-18C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-18C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-18C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-18C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-18C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-18C>G
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-18C>G
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10236
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 13701
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5022
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

19-32954759-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32954759
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 32954759
    reference: chr 19
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000465997
  ensembl transcript: ENST00000588648
  gene symbol: DPY19L3
  hgvsc: ENST00000588648.3:c.745-16G>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000590651
  gene symbol: DPY19L3
  hgvsc: ENST00000590651.1:n.165-16G>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000344937
  ensembl transcript: ENST00000342179
  gene symbol: DPY19L3
  hgvsc: ENST00000342179.5:c.1446-16G>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000474174
  ensembl transcript: ENST00000592832
  gene symbol: DPY19L3
  hgvsc: ENST00000592832.2:c.230-16G>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000466086
  ensembl transcript: ENST00000586987
  gene symbol: DPY19L3
  hgvsc: ENST00000586987.1:c.1446-16G>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl protein: ENSP00000376081
  ensembl transcript: ENST00000392250
  gene symbol: DPY19L3
  hgvsc: ENST00000392250.2:c.1446-16G>T
  variant of: http://identifiers.org/hgnc/27120
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178904
  ensembl transcript: ENST00000592142
  gene symbol: DPY19L3
  hgvsc: ENST00000592142.1:n.359-16G>T
  variant of: http://identifiers.org/hgnc/27120
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4375
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5026
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

20-44037551-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037551
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037551
    reference: chr 20
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.250G>T
  hgvsp: ENSP00000361807.3:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*256G>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.544G>T
  hgvsp: ENSP00000361805.3:p.Asp182Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.250G>T
  hgvsp: ENSP00000354250.4:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.250G>T
  hgvsp: ENSP00000361797.2:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*251G>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.250G>T
  hgvsp: ENSP00000361802.1:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*251G>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.426G>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.429G>T
  hgvsp: ENSP00000414161.1:p.Asp144Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.250G>T
  hgvsp: ENSP00000349822.2:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.250G>T
  hgvsp: ENSP00000361808.3:p.Asp84Tyr
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.556G>T
  hgvsp: ENSP00000361795.3:p.Asp186Tyr
  variant of: http://identifiers.org/hgnc/15881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp186Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-44037552-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037552
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037552
    reference: chr 20
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.251A>G
  hgvsp: ENSP00000361808.3:p.Asp84Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*252A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.545A>G
  hgvsp: ENSP00000361805.3:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.251A>G
  hgvsp: ENSP00000361802.1:p.Asp84Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.427A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.251A>G
  hgvsp: ENSP00000349822.2:p.Asp84Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.251A>G
  hgvsp: ENSP00000354250.4:p.Asp84Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.557A>G
  hgvsp: ENSP00000361795.3:p.Asp186Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.251A>G
  hgvsp: ENSP00000361807.3:p.Asp84Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.251A>G
  hgvsp: ENSP00000361797.2:p.Asp84Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.430A>G
  hgvsp: ENSP00000414161.1:p.Asp144Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*257A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*252A>G
  variant of: http://identifiers.org/hgnc/33535
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp186Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

20-44037553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037553
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037553
    reference: chr 20
allele count: 4
allele frequency: 3.312519668085529e-5
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.431T>C
  hgvsp: ENST00000443296.1:c.431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.252T>C
  hgvsp: ENST00000372717.1:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.558T>C
  hgvsp: ENST00000372710.3:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.252T>C
  hgvsp: ENST00000372722.3:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.252T>C
  hgvsp: ENST00000360981.4:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.546T>C
  hgvsp: ENST00000372720.3:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.428T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.252T>C
  hgvsp: ENST00000372712.2:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.252T>C
  hgvsp: ENST00000357275.2:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*253T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.252T>C
  hgvsp: ENST00000372723.3:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*253T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*258T>C
  variant of: http://identifiers.org/hgnc/33535
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp186Asp
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

20-44037557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037557
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037557
    reference: chr 20
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.550C>T
  hgvsp: ENSP00000361805.3:p.Pro184Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.256C>T
  hgvsp: ENSP00000361807.3:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.256C>T
  hgvsp: ENSP00000349822.2:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.432C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.435C>T
  hgvsp: ENSP00000414161.1:p.Pro146Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*257C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.256C>T
  hgvsp: ENSP00000361808.3:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.256C>T
  hgvsp: ENSP00000354250.4:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.256C>T
  hgvsp: ENSP00000361802.1:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*257C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.256C>T
  hgvsp: ENSP00000361797.2:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*262C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.562C>T
  hgvsp: ENSP00000361795.3:p.Pro188Ser
  variant of: http://identifiers.org/hgnc/15881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro188Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ

20-44037568-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037568
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037568
    reference: chr 20
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.267C>G
  hgvsp: ENST00000372717.1:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.446C>G
  hgvsp: ENST00000443296.1:c.446C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*273C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.573C>G
  hgvsp: ENST00000372710.3:c.573C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.561C>G
  hgvsp: ENST00000372720.3:c.561C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.267C>G
  hgvsp: ENST00000372723.3:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.267C>G
  hgvsp: ENST00000372712.2:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.267C>G
  hgvsp: ENST00000372722.3:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*268C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.267C>G
  hgvsp: ENST00000360981.4:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*268C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.267C>G
  hgvsp: ENST00000357275.2:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.443C>G
  variant of: http://identifiers.org/hgnc/33535
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro191Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/20-44037569-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037569
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037569
    reference: chr 20
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.268C>A
  hgvsp: ENSP00000361802.1:p.Gln90Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.268C>A
  hgvsp: ENSP00000361807.3:p.Gln90Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.268C>A
  hgvsp: ENSP00000361797.2:p.Gln90Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.268C>A
  hgvsp: ENSP00000349822.2:p.Gln90Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.268C>A
  hgvsp: ENSP00000361808.3:p.Gln90Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.447C>A
  hgvsp: ENSP00000414161.1:p.Gln150Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*269C>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.562C>A
  hgvsp: ENSP00000361805.3:p.Gln188Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*274C>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*269C>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.268C>A
  hgvsp: ENSP00000354250.4:p.Gln90Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.574C>A
  hgvsp: ENSP00000361795.3:p.Gln192Lys
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.444C>A
  variant of: http://identifiers.org/hgnc/33535
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln192Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

20-44037570-AGTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037570
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037567
    reference: chr 20
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.449_451delGTC
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*279_*281delGTC
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*274_*276delGTC
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*274_*276delGTC
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.273_275delGTC
  hgvsp: ENSP00000361808.3:p.Ser92del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.567_569delGTC
  hgvsp: ENSP00000361805.3:p.Ser190del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.273_275delGTC
  hgvsp: ENSP00000349822.2:p.Ser92del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.273_275delGTC
  hgvsp: ENSP00000354250.4:p.Ser92del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.452_454delGTC
  hgvsp: ENSP00000414161.1:p.Ser152del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.273_275delGTC
  hgvsp: ENSP00000361797.2:p.Ser92del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.273_275delGTC
  hgvsp: ENSP00000361802.1:p.Ser92del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.273_275delGTC
  hgvsp: ENSP00000361807.3:p.Ser92del
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.579_581delGTC
  hgvsp: ENSP00000361795.3:p.Ser194del
  variant of: http://identifiers.org/hgnc/15881
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10692
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser194del
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: AGTC
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

20-44037571-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037571
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037571
    reference: chr 20
allele count: 13
allele frequency: 1.076675887429395e-4
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.270G>A
  hgvsp: ENST00000372722.3:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.270G>A
  hgvsp: ENST00000372712.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.270G>A
  hgvsp: ENST00000357275.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.564G>A
  hgvsp: ENST00000372720.3:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.270G>A
  hgvsp: ENST00000360981.4:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.270G>A
  hgvsp: ENST00000372717.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.449G>A
  hgvsp: ENST00000443296.1:c.449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*271G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.446G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*276G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.576G>A
  hgvsp: ENST00000372710.3:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*271G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.270G>A
  hgvsp: ENST00000372723.3:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln192Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

20-44037573-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037573
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037573
    reference: chr 20
allele count: 2
allele frequency: 1.656424442199069e-5
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.272C>T
  hgvsp: ENSP00000361807.3:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.272C>T
  hgvsp: ENSP00000349822.2:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.451C>T
  hgvsp: ENSP00000414161.1:p.Ser151Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.272C>T
  hgvsp: ENSP00000361808.3:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.578C>T
  hgvsp: ENSP00000361795.3:p.Ser193Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.272C>T
  hgvsp: ENSP00000354250.4:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.272C>T
  hgvsp: ENSP00000361802.1:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.448C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*278C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.566C>T
  hgvsp: ENSP00000361805.3:p.Ser189Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.272C>T
  hgvsp: ENSP00000361797.2:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/15881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser193Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

20-44037574-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037574
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037574
    reference: chr 20
allele count: 9
allele frequency: 7.454033460327978e-5
allele num: 120740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.273G>A
  hgvsp: ENST00000372723.3:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.273G>A
  hgvsp: ENST00000360981.4:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*274G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.567G>A
  hgvsp: ENST00000372720.3:c.567G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.452G>A
  hgvsp: ENST00000443296.1:c.452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.449G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.579G>A
  hgvsp: ENST00000372710.3:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.273G>A
  hgvsp: ENST00000372722.3:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.273G>A
  hgvsp: ENST00000372717.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.273G>A
  hgvsp: ENST00000357275.2:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.273G>A
  hgvsp: ENST00000372712.2:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*279G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*274G>A
  variant of: http://identifiers.org/hgnc/33535
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser193Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

20-44037580-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037580
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037580
    reference: chr 20
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+2T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.279T>C
  hgvsp: ENST00000372722.3:c.279T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.458T>C
  hgvsp: ENST00000443296.1:c.458T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+2T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+2T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+2T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+2T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+2T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+2T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.279T>C
  hgvsp: ENST00000372717.1:c.279T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+2T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+2T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+2T>C
  variant of: http://identifiers.org/hgnc/15881
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.583+2T>C
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

20-44037585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037585
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037585
    reference: chr 20
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.284C>T
  hgvsp: ENSP00000361807.3:p.Pro95Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+7C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+7C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+7C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.284C>T
  hgvsp: ENSP00000361802.1:p.Pro95Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+7C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+7C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+7C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+7C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+7C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+7C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.463C>T
  hgvsp: ENSP00000414161.1:p.Pro155Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+7C>T
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro95Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

20-44037589-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037589
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037589
    reference: chr 20
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+11C>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.288C>G
  hgvsp: ENST00000372722.3:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+11C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+11C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.288C>G
  hgvsp: ENST00000372717.1:c.288C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.467C>G
  hgvsp: ENST00000443296.1:c.467C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+11C>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+11C>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+11C>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+11C>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+11C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+11C>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+11C>G
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu96Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

20-44037590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037590
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037590
    reference: chr 20
allele count: 2
allele frequency: 1.656891009709381e-5
allele num: 120708
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+12T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+12T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.289T>C
  hgvsp: ENSP00000361807.3:p.Cys97Arg
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.468T>C
  hgvsp: ENSP00000414161.1:p.Cys157Arg
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+12T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.289T>C
  hgvsp: ENSP00000361802.1:p.Cys97Arg
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+12T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+12T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+12T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+12T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+12T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+12T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+12T>C
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys97Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

20-44037605-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037605
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037605
    reference: chr 20
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+27A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.483A>G
  hgvsp: ENSP00000414161.1:p.Ser162Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+27A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+27A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.304A>G
  hgvsp: ENSP00000361807.3:p.Ser102Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+27A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+27A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+27A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+27A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.304A>G
  hgvsp: ENSP00000361802.1:p.Ser102Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+27A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+27A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+27A>G
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser102Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

20-44037611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037611
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037611
    reference: chr 20
allele count: 8
allele frequency: 6.6333891643588e-5
allele num: 120602
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+33A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.489A>G
  hgvsp: ENSP00000414161.1:p.Ser164Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+33A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+33A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+33A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+33A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+33A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+33A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+33A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+33A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.310A>G
  hgvsp: ENSP00000361807.3:p.Ser104Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.310A>G
  hgvsp: ENSP00000361802.1:p.Ser104Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+33A>G
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ser104Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

20-44037624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037624
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037624
    reference: chr 20
allele count: 2
allele frequency: 1.659916340216453e-5
allele num: 120488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+46C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.502C>T
  hgvsp: ENSP00000414161.1:p.Pro168Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.323C>T
  hgvsp: ENSP00000361807.3:p.Pro108Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.323C>T
  hgvsp: ENSP00000361802.1:p.Pro108Leu
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+46C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+46C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+46C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+46C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+46C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+46C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+46C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+46C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+46C>T
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro108Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

20-44037625-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037625
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037625
    reference: chr 20
allele count: 13
allele frequency: 1.079053089411999e-4
allele num: 120476
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+47G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.324G>A
  hgvsp: ENST00000372722.3:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+47G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+47G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+47G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+47G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+47G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+47G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.324G>A
  hgvsp: ENST00000372717.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.503G>A
  hgvsp: ENST00000443296.1:c.503G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+47G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+47G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+47G>A
  variant of: http://identifiers.org/hgnc/33535
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro108Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

20-44037625-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037625
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037625
    reference: chr 20
allele count: 4
allele frequency: 3.32016335203692e-5
allele num: 120476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+47G>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+47G>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.324G>C
  hgvsp: ENST00000372722.3:c.324G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+47G>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+47G>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+47G>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.503G>C
  hgvsp: ENST00000443296.1:c.503G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+47G>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+47G>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+47G>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.324G>C
  hgvsp: ENST00000372717.1:c.324G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+47G>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+47G>C
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro108Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-44037627-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037627
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037627
    reference: chr 20
allele count: 1
allele frequency: 8.30137304710199e-6
allele num: 120462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.326A>C
  hgvsp: ENSP00000361807.3:p.Asp109Ala
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.505A>C
  hgvsp: ENSP00000414161.1:p.Asp169Ala
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+49A>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+49A>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+49A>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+49A>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+49A>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+49A>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.326A>C
  hgvsp: ENSP00000361802.1:p.Asp109Ala
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+49A>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+49A>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+49A>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+49A>C
  variant of: http://identifiers.org/hgnc/33535
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp109Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

20-44037632-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037632
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037632
    reference: chr 20
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+54A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+54A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.510A>G
  hgvsp: ENSP00000414161.1:p.Arg171Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+54A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+54A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+54A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+54A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+54A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.331A>G
  hgvsp: ENSP00000361802.1:p.Arg111Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.331A>G
  hgvsp: ENSP00000361807.3:p.Arg111Gly
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+54A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+54A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+54A>G
  variant of: http://identifiers.org/hgnc/33535
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg111Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

20-44037638-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037638
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037638
    reference: chr 20
allele count: 2
allele frequency: 1.66267624368183e-5
allele num: 120288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+60T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+60T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+60T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+60T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.337T>C
  hgvsp: ENSP00000361807.3:p.Ter113ArgextTer21
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+60T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.337T>C
  hgvsp: ENSP00000361802.1:p.Ter113ArgextTer21
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+60T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+60T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.516T>C
  hgvsp: ENSP00000414161.1:p.Ter173ArgextTer21
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+60T>C
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+60T>C
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+60T>C
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter113ArgextTer21
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

20-44037643-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037643
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037643
    reference: chr 20
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+65C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+65C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+65C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+65C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+65C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+65C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+65C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+65C>T
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+65C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.*3C>T
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+65C>T
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

20-44037644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037644
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037644
    reference: chr 20
allele count: 88
allele frequency: 7.326617267504787e-4
allele num: 120110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+66G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+66G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.*4G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+66G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+66G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+66G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+66G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+66G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+66G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+66G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+66G>A
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24662
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP

20-44037652-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037652
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037652
    reference: chr 20
allele count: 1
allele frequency: 8.339170752860335e-6
allele num: 119916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+74A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+74A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+74A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.*12A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+74A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.*12A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+74A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+74A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.*12A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+74A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+74A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+74A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+74A>G
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

20-44037653-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037653
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037653
    reference: chr 20
allele count: 1
allele frequency: 8.342231713828083e-6
allele num: 119872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+75A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+75A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.*13A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.*13A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+75A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.*13A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+75A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+75A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+75A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+75A>G
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+75A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+75A>G
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+75A>G
  variant of: http://identifiers.org/hgnc/15881
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18027
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

20-44037663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037663
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037663
    reference: chr 20
allele count: 1
allele frequency: 8.377454594196099e-6
allele num: 119368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+85G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.*23G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.*23G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+85G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+85G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+85G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+85G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.*23G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+85G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+85G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+85G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+85G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+85G>A
  variant of: http://identifiers.org/hgnc/33535
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23431
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

20-44037682-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44037682
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 44037682
    reference: chr 20
allele count: 1
allele frequency: 8.467974121871083e-6
allele num: 118092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361802
  ensembl transcript: ENST00000372717
  gene symbol: DBNDD2
  hgvsc: ENST00000372717.1:c.*36+6G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl transcript: ENST00000475242
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000475242.1:n.453+104G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000354250
  ensembl transcript: ENST00000360981
  gene symbol: DBNDD2
  hgvsc: ENST00000360981.4:c.277+104G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361795
  ensembl transcript: ENST00000372710
  gene symbol: DBNDD2
  hgvsc: ENST00000372710.3:c.583+104G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000456116
  ensembl transcript: ENST00000419593
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000419593.1:c.*278+104G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361808
  ensembl transcript: ENST00000372723
  gene symbol: DBNDD2
  hgvsc: ENST00000372723.3:c.277+104G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361797
  ensembl transcript: ENST00000372712
  gene symbol: DBNDD2
  hgvsc: ENST00000372712.2:c.277+104G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361805
  ensembl transcript: ENST00000372720
  gene symbol: DBNDD2
  hgvsc: ENST00000372720.3:c.571+104G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000361807
  ensembl transcript: ENST00000372722
  gene symbol: DBNDD2
  hgvsc: ENST00000372722.3:c.*36+6G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000414161
  ensembl transcript: ENST00000443296
  gene symbol: DBNDD2
  hgvsc: ENST00000443296.1:c.*36+6G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000244274
  ensembl protein: ENSP00000349822
  ensembl transcript: ENST00000357275
  gene symbol: DBNDD2
  hgvsc: ENST00000357275.2:c.277+104G>A
  variant of: http://identifiers.org/hgnc/15881
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457650
  ensembl transcript: ENST00000452133
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000452133.1:c.*278+104G>A
  variant of: http://identifiers.org/hgnc/33535
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254806
  ensembl protein: ENSP00000457768
  ensembl transcript: ENST00000458187
  gene symbol: SYS1-DBNDD2
  hgvsc: ENST00000458187.1:c.*283+104G>A
  variant of: http://identifiers.org/hgnc/33535
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15243
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*36+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6625
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7618
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3267
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29477
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578432301038608e-5
allele num: 63354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.715e0

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.708664e6

FS
type: SiteQuality
SIO_000300: 5.284e0

MQ
type: SiteQuality
SIO_000300: 5.02e1

QD
type: SiteQuality
SIO_000300: 6.29e0

GenotypeQuality
all individuals: 665
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29477
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.945598417408506e-4
allele num: 8088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 5.284e0

QD
type: SiteQuality
SIO_000300: 6.29e0

MQRankSum
type: SiteQuality
SIO_000300: -3.715e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

DP
type: SiteQuality
SIO_000300: 1.708664e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.02e1

GenotypeQuality
all individuals: 503
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 268
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.338551859099804e-4
allele num: 8176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 9.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.721688e6

MQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
all individuals: 2169
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1389
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7650
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566661444461852e-5
allele num: 63830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 9.66e-1

DP
type: SiteQuality
SIO_000300: 1.721688e6

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
all individuals: 1897
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 30874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7662
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 745
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
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: 1
allele frequency: 1.21153380179307e-4
allele num: 8254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64164
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.619e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.184e0

MQ
type: SiteQuality
SIO_000300: 5.801e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.731766e6

QD
type: SiteQuality
SIO_000300: 1.018e1

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

GenotypeQuality
all individuals: 2640
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1210
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7747
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516438189979376e-5
allele num: 65944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
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: 894
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-1

QD
type: SiteQuality
SIO_000300: 8.4e0

DP
type: SiteQuality
SIO_000300: 1.774307e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.36e0

MQRankSum
type: SiteQuality
SIO_000300: -3.75e-1

FS
type: SiteQuality
SIO_000300: 3.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

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: 3

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: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
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: 3
allele frequency: 2.610511660285416e-4
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.792044e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.579e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.755e-1

DP
type: SiteQuality
SIO_000300: 1.79351e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.047e0

MQRankSum
type: SiteQuality
SIO_000300: 9.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.841e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.93050193050193e-4
allele num: 10360
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.173e0

DP
type: SiteQuality
SIO_000300: 1.793871e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.018e0

FS
type: SiteQuality
SIO_000300: 2.0013e1

MQRankSum
type: SiteQuality
SIO_000300: -1.138e0

QD
type: SiteQuality
SIO_000300: 1.427e1

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

East Asian
type: Population
allele count: 7
allele frequency: 8.107482047718323e-4
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.895193977996526e-4
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.795414e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

FS
type: SiteQuality
SIO_000300: 1.429e0

QD
type: SiteQuality
SIO_000300: 1.456e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.125e0

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: 20

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 19
allele frequency: 1.833269008104979e-3
allele num: 10364
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.76e-1

DP
type: SiteQuality
SIO_000300: 1.797148e6

FS
type: SiteQuality
SIO_000300: 1.493e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

QD
type: SiteQuality
SIO_000300: 1.408e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

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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variant carriers: 0

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

Latino
type: Population
allele count: 55
allele frequency: 4.774305555555556e-3
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

FS
type: SiteQuality
SIO_000300: 7.55e-1

DP
type: SiteQuality
SIO_000300: 1.801474e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.229e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1312
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.989e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.802722e6

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.95e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 1625
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.803e0

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

FS
type: SiteQuality
SIO_000300: 3.989e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.802722e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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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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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.929e1

FS
type: SiteQuality
SIO_000300: 3.68e0

DP
type: SiteQuality
SIO_000300: 1.802867e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 2803
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7931
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32763
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.597852441981296e-4
allele num: 11548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.994693131052679e-5
allele num: 66706
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 1.274e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.445e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

DP
type: SiteQuality
SIO_000300: 1.803386e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.323e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

GenotypeQuality
all individuals: 3840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 32758
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

FS
type: SiteQuality
SIO_000300: 1.824e0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.803472e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 1315
bin: 8.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 7421
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
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: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.343e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

DP
type: SiteQuality
SIO_000300: 1.803887e6

MQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

FS
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2911
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1626
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3838
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variant carriers: 0

GenotypeQuality
all individuals: 7421
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.107e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

FS
type: SiteQuality
SIO_000300: 6.57e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.804023e6

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1315
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variant carriers: 0

GenotypeQuality
all individuals: 7933
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variant carriers: 2

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

GenotypeQuality
all individuals: 2808
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variant carriers: 0

GenotypeQuality
all individuals: 7424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3838
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.32e-1

DP
type: SiteQuality
SIO_000300: 1.804305e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.257e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e0

VQSLOD
type: SiteQuality
SIO_000300: 8.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.97e-1

QD
type: SiteQuality
SIO_000300: 1.489e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

GenotypeQuality
all individuals: 2808
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1626
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

DP
type: SiteQuality
SIO_000300: 1.804294e6

VQSLOD
type: SiteQuality
SIO_000300: -1.092e0

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

FS
type: SiteQuality
SIO_000300: 1.1071e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.469e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3836
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variant carriers: 0

GenotypeQuality
all individuals: 1316
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.09819555182543e-4
allele num: 66724
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

FS
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 1.80564e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.411e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.152e1

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 29
allele frequency: 2.787925398961738e-3
allele num: 10402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

DP
type: SiteQuality
SIO_000300: 1.808051e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.33e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.19e-1

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 50
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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: 7960
bin: 9.75e1
variant carriers: 1

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.121e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

DP
type: SiteQuality
SIO_000300: 1.79767e6

QD
type: SiteQuality
SIO_000300: 1.392e1

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
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GenotypeQuality
all individuals: 22
bin: 4.25e1
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GenotypeQuality
all individuals: 3801
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GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32211
bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e0

FS
type: SiteQuality
SIO_000300: 5.083e0

VQSLOD
type: SiteQuality
SIO_000300: -9.373e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.128e1

DP
type: SiteQuality
SIO_000300: 1.793642e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.272e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 7247
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GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.793568e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.96e-1

MQ
type: SiteQuality
SIO_000300: 6.052e1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.5e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.38e-1

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

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.503e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.052e0

QD
type: SiteQuality
SIO_000300: 1.676e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.449999999999999e0

DP
type: SiteQuality
SIO_000300: 1.788946e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7958
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.801e0

QD
type: SiteQuality
SIO_000300: 1.629e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.624e-1

DP
type: SiteQuality
SIO_000300: 1.766286e6

FS
type: SiteQuality
SIO_000300: 1.866e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 1619
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1309
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 705
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variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.132711885195633e-5
allele num: 16306
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.99e0

DP
type: SiteQuality
SIO_000300: 1.764934e6

FS
type: SiteQuality
SIO_000300: 1.952e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.389e0

GenotypeQuality
all individuals: 2758
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
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GenotypeQuality
all individuals: 7962
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 422
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GenotypeQuality
all individuals: 1618
bin: 9.25e1
variant carriers: 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: 66536
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.847063169560399e-4
allele num: 16242
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.76158e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.27e-1

QD
type: SiteQuality
SIO_000300: 1.364e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

GenotypeQuality
all individuals: 1308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
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variant carriers: 0

GenotypeQuality
all individuals: 29433
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.606e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.236e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.217e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

DP
type: SiteQuality
SIO_000300: 1.761152e6

GenotypeQuality
all individuals: 774
bin: 9.25e1
variant carriers: 161

GenotypeQuality
all individuals: 1205
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variant carriers: 223

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 10

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 195

GenotypeQuality
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variant carriers: 110

GenotypeQuality
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variant carriers: 112

GenotypeQuality
all individuals: 1016
bin: 8.25e1
variant carriers: 175

GenotypeQuality
all individuals: 51032
bin: 9.75e1
variant carriers: 47873

African
type: Population
allele count: 4813
allele frequency: 4.626994808690637e-1
allele num: 10402
num of homozygotes: 1101

East Asian
type: Population
allele count: 5455
allele frequency: 6.312196250867854e-1
allele num: 8642
num of homozygotes: 1716

Latino
type: Population
allele count: 4449
allele frequency: 3.845954356846473e-1
allele num: 11568
num of homozygotes: 891

European (Finnish)
type: Population
allele count: 4109
allele frequency: 6.216338880484115e-1
allele num: 6610
num of homozygotes: 1269

European (Non-Finnish)
type: Population
allele count: 41952
allele frequency: 6.297964330751216e-1
allele num: 66612
num of homozygotes: 13269

South Asian
type: Population
allele count: 9516
allele frequency: 5.791139240506329e-1
allele num: 16432
num of homozygotes: 2820

Other
type: Population
allele count: 536
allele frequency: 5.916114790286976e-1
allele num: 906
num of homozygotes: 161

ClippingRankSum
type: SiteQuality
SIO_000300: -4.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.51e-2

QD
type: SiteQuality
SIO_000300: 2.345e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.217e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 5.944722e6

GenotypeQuality
all individuals: 15792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3455
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GenotypeQuality
all individuals: 2992
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2098
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GenotypeQuality
all individuals: 260
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.083465141744738e-5
allele num: 16438
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

FS
type: SiteQuality
SIO_000300: 3.196e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.183e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 2.562199e6

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5000
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GenotypeQuality
all individuals: 15962
bin: 6.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

FS
type: SiteQuality
SIO_000300: 4.712e0

DP
type: SiteQuality
SIO_000300: 2.562988e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: -1.487e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.614e0

QD
type: SiteQuality
SIO_000300: 1.868e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

GenotypeQuality
all individuals: 3452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2995
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7581
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 200
allele frequency: 1.922337562475971e-2
allele num: 10404
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50220608097968e-5
allele num: 66634
num of homozygotes: 0

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

Latino
type: Population
allele count: 13
allele frequency: 1.123595505617978e-3
allele num: 11570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

DP
type: SiteQuality
SIO_000300: 2.568924e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.892e0

QD
type: SiteQuality
SIO_000300: 1.425e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.71e0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7643
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.870000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

DP
type: SiteQuality
SIO_000300: 2.554288e6

QD
type: SiteQuality
SIO_000300: 1.373e1

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

GenotypeQuality
all individuals: 2106
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00048007681229e-5
allele num: 66656
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.345e0

QD
type: SiteQuality
SIO_000300: 1.267e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 2.245e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

DP
type: SiteQuality
SIO_000300: 2.554929e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

QD
type: SiteQuality
SIO_000300: 1.323e1

DP
type: SiteQuality
SIO_000300: 2.556095e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.076e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

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

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5019
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7684
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 1.374e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

QD
type: SiteQuality
SIO_000300: 1.462e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.556923e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.109999999999999e0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18162
bin: 9.75e1
variant carriers: 39

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16695
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 36
allele frequency: 2.182347235693501e-3
allele num: 16496
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.209e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 6.57e-1

DP
type: SiteQuality
SIO_000300: 2.558861e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.737e0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7702
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3462
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18127
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2105
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 66674
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.556253e6

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 5.649e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.222e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 1.155e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

GenotypeDepth
all individuals: 1088
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2813
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
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GenotypeQuality
all individuals: 863
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 1832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2838
bin: 7.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

DP
type: SiteQuality
SIO_000300: 1.680753e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.858e0

FS
type: SiteQuality
SIO_000300: 3.594e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

GenotypeDepth
all individuals: 53
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 80
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 576
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25154
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 8.25e1
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
all individuals: 12
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GenotypeQuality
all individuals: 863
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GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 2593
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2838
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 38903
bin: 6.25e1
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GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.77e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

VQSLOD
type: SiteQuality
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele num: 66728
num of homozygotes: 0

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

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

Other
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East Asian
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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Other
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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South Asian
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VQSLOD
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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Latino
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African
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South Asian
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.1102e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.5e0

VQSLOD
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SIO_000300: -1.185e0

BaseQRankSum
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SIO_000300: 5.0e-1

ClippingRankSum
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SIO_000300: -2.159e0

QD
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SIO_000300: 2.004e1

DP
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SIO_000300: 1.68033e6

MQRankSum
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SIO_000300: -1.27e-1

InbreedingCoeff
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SIO_000300: 3.98e-2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
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allele count: 6
allele frequency: 8.992266650680415e-5
allele num: 66724
num of homozygotes: 0

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

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

Latino
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allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

Other
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South Asian
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allele frequency: 0.0e0
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FS
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.8e-3

VQSLOD
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MQ
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SIO_000300: 5.966e1

ReadPosRankSum
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SIO_000300: 9.12e-1

QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

BaseQRankSum
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SIO_000300: 4.86e0

VQSLOD
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SIO_000300: 5.71e-1

ClippingRankSum
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SIO_000300: -1.407e0

InbreedingCoeff
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SIO_000300: 2.7e-3

MQ
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SIO_000300: 5.962e1

MQRankSum
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SIO_000300: -2.28e-1

DP
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SIO_000300: 1.680011e6

FS
type: SiteQuality
SIO_000300: 1.794e0

QD
type: SiteQuality
SIO_000300: 1.299e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

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

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

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
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num of homozygotes: 0

MQ
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SIO_000300: 5.886e1

QD
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SIO_000300: 1.122e1

BaseQRankSum
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SIO_000300: -8.699999999999999e-2

MQRankSum
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SIO_000300: -7.000000000000001e-2

InbreedingCoeff
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SIO_000300: 2.9e-3

FS
type: SiteQuality
SIO_000300: 8.159999999999999e-1

DP
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SIO_000300: 1.679838e6

VQSLOD
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SIO_000300: -3.909e-1

ReadPosRankSum
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SIO_000300: -3.09e-1

ClippingRankSum
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SIO_000300: 6.23e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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African
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allele num: 9788
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Latino
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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SIO_000300: -4.71e-1

ClippingRankSum
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SIO_000300: -8.71e-1

VQSLOD
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GenotypeDepth
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variant carriers: 0

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

South Asian
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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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Latino
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Other
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

African
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BaseQRankSum
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FS
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VQSLOD
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DP
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

African
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allele count: 0
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Other
type: Population
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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DP
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SIO_000300: 1.678012e6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 8
allele frequency: 9.289363678588017e-4
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

Other
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Latino
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DP
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 5.3e0

InbreedingCoeff
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SIO_000300: 4.1e-3

VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
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FS
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DP
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ClippingRankSum
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SIO_000300: 4.0e-1

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

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

East Asian
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allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 11
allele frequency: 1.652346331791143e-4
allele num: 66572
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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InbreedingCoeff
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DP
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ClippingRankSum
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FS
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QD
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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

African
type: Population
allele count: 1
allele frequency: 1.027115858668858e-4
allele num: 9736
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.506399086703119e-5
allele num: 66572
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South Asian
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Other
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66570
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South Asian
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African
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Latino
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East Asian
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Other
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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FS
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QD
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503262078710802e-5
allele num: 66522
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Latino
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FS
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 892
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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

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

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

Latino
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allele count: 2
allele frequency: 1.732201628269531e-4
allele num: 11546
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.912e0

VQSLOD
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SIO_000300: 8.139999999999999e-1

MQRankSum
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SIO_000300: 7.22e-1

InbreedingCoeff
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SIO_000300: 3.4e-3

ReadPosRankSum
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SIO_000300: 1.2e0

ClippingRankSum
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SIO_000300: -4.3e-2

BaseQRankSum
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QD
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SIO_000300: 1.303e1

DP
type: SiteQuality
SIO_000300: 1.669386e6

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

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

Other
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 3.32e-1

InbreedingCoeff
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SIO_000300: 3.1e-3

VQSLOD
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SIO_000300: -8.055e-1

DP
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SIO_000300: 1.665542e6

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.03498240529911e-4
allele num: 9662
num of homozygotes: 0

South Asian
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allele count: 7
allele frequency: 4.251184258472003e-4
allele num: 16466
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.02663773880552e-5
allele num: 66372
num of homozygotes: 0

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

East Asian
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allele count: 75
allele frequency: 8.729050279329608e-3
allele num: 8592
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -7.4e-2

VQSLOD
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SIO_000300: 4.22e0

ReadPosRankSum
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SIO_000300: 3.08e-1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.18e-2

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.108e0

DP
type: SiteQuality
SIO_000300: 1.66561e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.653456e6

VQSLOD
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SIO_000300: 6.78e-1

MQ
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SIO_000300: 5.939e1

InbreedingCoeff
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SIO_000300: 1.9e-3

ReadPosRankSum
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MQRankSum
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QD
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SIO_000300: 1.439e1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 3.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11510
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66240
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele num: 16448
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6592
num of homozygotes: 0

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

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

Other
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South Asian
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allele frequency: 6.095330976472023e-5
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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MQ
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.535202186127913e-5
allele num: 65138
num of homozygotes: 0

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

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

South Asian
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ClippingRankSum
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SIO_000300: -1.418e0