8-74706376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706376
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706376
    reference: chr 8
allele count: 2
allele frequency: 1.882282078792328e-5
allele num: 106254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11510T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11510T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-26T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11510T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7591
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18240
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

8-74706379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706379
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706379
    reference: chr 8
allele count: 1
allele frequency: 9.477056047309464e-6
allele num: 105518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11507T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11507T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-29T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11507T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9744
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

8-74706386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706386
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706386
    reference: chr 8
allele count: 7
allele frequency: 6.797700435052828e-5
allele num: 102976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11500G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-36G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11500G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11500G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18932
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12986
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13117
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

8-74706388-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706388
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706388
    reference: chr 8
allele count: 527
allele frequency: 5.187314211469181e-3
allele num: 101594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11498T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11498T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-38T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11498T>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 2.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 2.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 18415
  bin: 1.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 14212
  bin: 1.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4900
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 8.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 4
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

8-74706389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706389
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706389
    reference: chr 8
allele count: 1
allele frequency: 9.875177753199558e-6
allele num: 101264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-39C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11497C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-39C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-39C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-39C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-39C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-39C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11497C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11497C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-39C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14164
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-74706395-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706395
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706395
    reference: chr 8
allele count: 1
allele frequency: 1.004722194313272e-5
allele num: 99530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11491T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11491T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-45T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11491T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13831
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4930
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4527
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

8-74706396-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706396
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706396
    reference: chr 8
allele count: 1
allele frequency: 1.010080604432234e-5
allele num: 99002
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-46A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-46A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-46A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-46A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-46A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-46A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11490A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11490A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11490A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-46A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4433
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-74706396-T-TAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706396
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706398
    reference: chr 8
allele count: 1
allele frequency: 1.010080604432234e-5
allele num: 99002
alternate allele: TAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-48_*281-47dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-48_443-47dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-48_563-47dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-48_530-47dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11488_429+11489dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-48_*157-47dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11488_442+11489dupTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11488_442+11489dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-48_476-47dupTT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-48_*241-47dupTT
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6733
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4527
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8350
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6800
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

8-74706399-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74706399
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74706399
    reference: chr 8
allele count: 1
allele frequency: 1.021366997589574e-5
allele num: 97908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*157-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.530-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.443-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.563-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.476-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*241-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+11487C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+11487C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*281-49C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+11487C>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17579
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3326
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-74717841-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717841
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717841
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 27066
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+45A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+45A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+45A>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16828
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

8-74717843-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717843
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717843
    reference: chr 8
allele count: 2
allele frequency: 7.379529186037931e-5
allele num: 27102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+43T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+43T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+43T>A
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17118
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5069
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20622
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

8-74717855-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717855
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717855
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 27970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+31A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+31A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+31A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22079
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19972
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-74717864-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717864
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717864
    reference: chr 8
allele count: 1
allele frequency: 3.429590506893477e-5
allele num: 29158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+22T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+22T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+22T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25974
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18819
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23336
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

8-74717865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717865
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717865
    reference: chr 8
allele count: 1
allele frequency: 3.419972640218878e-5
allele num: 29240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+21A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+21A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23679
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-74717867-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717867
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717867
    reference: chr 8
allele count: 1
allele frequency: 3.382263410674423e-5
allele num: 29566
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+19T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+19T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+19T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16193
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6441
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-74717878-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717878
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717878
    reference: chr 8
allele count: 1
allele frequency: 3.123048094940662e-5
allele num: 32020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+8G>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+8G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+8G>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.442+8G>C
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-74717879-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717879
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717879
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 32352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+7A>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+7A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+7A>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30785
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.442+7A>T
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

8-74717881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717881
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717881
    reference: chr 8
allele count: 1
allele frequency: 3.047851264858275e-5
allele num: 32810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.529+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.442+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.562+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.429+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*156+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*156+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.475+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.442+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*156+5G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.442+5G>A
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31072
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.442+5G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-74717887-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717887
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717887
    reference: chr 8
allele count: 1
allele frequency: 2.894356005788712e-5
allele num: 34550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.528T>C
  hgvsp: ENST00000517608.1:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.441T>C
  hgvsp: ENST00000453587.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.474T>C
  hgvsp: ENST00000602969.1:c.474T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.428T>C
  hgvsp: ENST00000523278.1:c.428T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*155T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.441T>C
  hgvsp: ENST00000602593.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*155T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*155T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.441T>C
  hgvsp: ENST00000358757.5:c.441T>C(p.%3D)
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.561T>C
  hgvsp: ENST00000419880.3:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31872
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.441T>C
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

8-74717888-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717888
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717888
    reference: chr 8
allele count: 1
allele frequency: 2.868288205598899e-5
allele num: 34864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.473A>G
  hgvsp: ENSP00000473516.1:p.His158Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.527A>G
  hgvsp: ENSP00000428813.2:p.His176Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.440A>G
  hgvsp: ENSP00000473561.1:p.His147Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.427A>G
  hgvsp: ENSP00000428835.1:p.His143Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*154A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.440A>G
  hgvsp: ENSP00000403764.2:p.His147Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.440A>G
  hgvsp: ENSP00000454445.2:p.His147Arg
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.560A>G
  hgvsp: ENSP00000397453.3:p.His187Arg
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His187Arg
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

8-74717903-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717903
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717903
    reference: chr 8
allele count: 1
allele frequency: 2.58224448690802e-5
allele num: 38726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*139C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.512C>T
  hgvsp: ENSP00000428813.2:p.Thr171Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.458C>T
  hgvsp: ENSP00000473516.1:p.Thr153Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.412C>T
  hgvsp: ENSP00000428835.1:p.Thr138Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.425C>T
  hgvsp: ENSP00000454445.2:p.Thr142Ile
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.425C>T
  hgvsp: ENSP00000473561.1:p.Thr142Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.545C>T
  hgvsp: ENSP00000397453.3:p.Thr182Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.425C>T
  hgvsp: ENSP00000403764.2:p.Thr142Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr182Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

8-74717911-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717911
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717911
    reference: chr 8
allele count: 3
allele frequency: 7.51503006012024e-5
allele num: 39920
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*131A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*131A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.417A>G
  hgvsp: ENST00000358757.5:c.417A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*131A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.417A>G
  hgvsp: ENST00000602593.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.504A>G
  hgvsp: ENST00000517608.1:c.504A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.450A>G
  hgvsp: ENST00000602969.1:c.450A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.404A>G
  hgvsp: ENST00000523278.1:c.404A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.537A>G
  hgvsp: ENST00000419880.3:c.537A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.417A>G
  hgvsp: ENST00000453587.2:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7998
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9375
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro179Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum

8-74717913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717913
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717913
    reference: chr 8
allele count: 1
allele frequency: 2.494512073438436e-5
allele num: 40088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.402C>T
  hgvsp: ENSP00000428835.1:p.Pro135Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.415C>T
  hgvsp: ENSP00000454445.2:p.Pro139Ser
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.535C>T
  hgvsp: ENSP00000397453.3:p.Pro179Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.502C>T
  hgvsp: ENSP00000428813.2:p.Pro168Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*129C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.415C>T
  hgvsp: ENSP00000473561.1:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*129C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*129C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.448C>T
  hgvsp: ENSP00000473516.1:p.Pro150Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.415C>T
  hgvsp: ENSP00000403764.2:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro179Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

8-74717918-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717918
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717918
    reference: chr 8
allele count: 1
allele frequency: 2.49488548475625e-5
allele num: 40082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.410A>G
  hgvsp: ENSP00000403764.2:p.Lys137Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.443A>G
  hgvsp: ENSP00000473516.1:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*124A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.530A>G
  hgvsp: ENSP00000397453.3:p.Lys177Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*124A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.497A>G
  hgvsp: ENSP00000428813.2:p.Lys166Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.410A>G
  hgvsp: ENSP00000473561.1:p.Lys137Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.410A>G
  hgvsp: ENSP00000454445.2:p.Lys137Arg
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.397A>G
  hgvsp: ENSP00000428835.1:p.Lys133Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*124A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys177Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-74717944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717944
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717944
    reference: chr 8
allele count: 1
allele frequency: 2.551801571909768e-5
allele num: 39188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*98T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*98T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.417T>C
  hgvsp: ENST00000602969.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.384T>C
  hgvsp: ENST00000358757.5:c.384T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.471T>C
  hgvsp: ENST00000517608.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.384T>C
  hgvsp: ENST00000602593.1:c.384T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.504T>C
  hgvsp: ENST00000419880.3:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*98T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.384T>C
  hgvsp: ENST00000453587.2:c.384T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.371T>C
  hgvsp: ENST00000523278.1:c.371T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29553
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn168Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-74717950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717950
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717950
    reference: chr 8
allele count: 5
allele frequency: 1.30684788290643e-4
allele num: 38260
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.378G>A
  hgvsp: ENST00000358757.5:c.378G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.411G>A
  hgvsp: ENST00000602969.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.378G>A
  hgvsp: ENST00000453587.2:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*92G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.465G>A
  hgvsp: ENST00000517608.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.498G>A
  hgvsp: ENST00000419880.3:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.378G>A
  hgvsp: ENST00000602593.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.365G>A
  hgvsp: ENST00000523278.1:c.365G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro166Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-74717951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717951
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717951
    reference: chr 8
allele count: 1
allele frequency: 2.608786392570176e-5
allele num: 38332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*91C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.497C>T
  hgvsp: ENSP00000397453.3:p.Pro166Leu
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*91C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.364C>T
  hgvsp: ENSP00000428835.1:p.Pro122Leu
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*91C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.377C>T
  hgvsp: ENSP00000454445.2:p.Pro126Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.377C>T
  hgvsp: ENSP00000473561.1:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.464C>T
  hgvsp: ENSP00000428813.2:p.Pro155Leu
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.410C>T
  hgvsp: ENSP00000473516.1:p.Pro137Leu
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.377C>T
  hgvsp: ENSP00000403764.2:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro166Leu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-74717953-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717953
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717953
    reference: chr 8
allele count: 3
allele frequency: 7.934408886537952e-5
allele num: 37810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.375A>G
  hgvsp: ENST00000453587.2:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.462A>G
  hgvsp: ENST00000517608.1:c.462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*89A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*89A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.362A>G
  hgvsp: ENST00000523278.1:c.362A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.495A>G
  hgvsp: ENST00000419880.3:c.495A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.375A>G
  hgvsp: ENST00000358757.5:c.375A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.375A>G
  hgvsp: ENST00000602593.1:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*89A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.408A>G
  hgvsp: ENST00000602969.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro165Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

8-74717971-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717971
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717971
    reference: chr 8
allele count: 1
allele frequency: 2.932551319648094e-5
allele num: 34100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-10T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-10T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-10T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21750
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

8-74717980-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717980
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717980
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 32516
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-19A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-19A>G
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17882
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23873
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15843
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

8-74717987-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717987
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717987
    reference: chr 8
allele count: 1
allele frequency: 3.252455603981006e-5
allele num: 30746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-26C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-26C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-26C>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12605
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

8-74717988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74717988
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74717988
    reference: chr 8
allele count: 557
allele frequency: 1.815870118015257e-2
allele num: 30674
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-27A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-27A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-27A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 1.25e1
  variant carriers: 248
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 2.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16208
  bin: 7.5e0
  variant carriers: 494
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25617
  bin: 2.5e0
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 4533
  bin: 6.25e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 28
num of homozygotes: 28
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

8-74718001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718001
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718001
    reference: chr 8
allele count: 1
allele frequency: 3.635041802980734e-5
allele num: 27510
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-40T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-40T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-40T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3577
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-74718003-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718003
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718003
    reference: chr 8
allele count: 1
allele frequency: 3.685684800235884e-5
allele num: 27132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-42T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-42T>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-42T>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27042
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5331
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

8-74718003-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718003
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718003
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 27132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-42T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-42T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-42T>A
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27042
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24673
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

8-74718004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718004
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718004
    reference: chr 8
allele count: 2
allele frequency: 7.422251911229867e-5
allele num: 26946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-43G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-43G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-43G>A
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27038
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2673
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

8-74718005-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718005
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718005
    reference: chr 8
allele count: 1
allele frequency: 3.738876841396844e-5
allele num: 26746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-44A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-44A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-44A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15680
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-74718006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718006
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718006
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 26748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-45C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-45C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-45C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27006
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15670
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

8-74718008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74718008
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74718008
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 26382
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.487-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.367-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.454-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.367-47C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.354-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*81-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.367-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*81-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.400-47C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*81-47C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15715
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4742
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5597
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

8-74722666-TGAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722666
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722662
    reference: chr 8
allele count: 5
allele frequency: 4.204365813460698e-5
allele num: 118924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.453+39_453+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.486+39_486+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.366+39_366+42delTTTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.366+39_366+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.399+39_399+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.353+39_353+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*80+39_*80+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*80+39_*80+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.366+39_366+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*80+39_*80+42delTTTC
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9823
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14824
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1719
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TGAAA
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-74722671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722671
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722671
    reference: chr 8
allele count: 8
allele frequency: 6.723932155524551e-5
allele num: 118978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*80+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.366+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.366+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.399+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.353+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*80+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.453+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.366+38C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.486+38C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*80+38C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

8-74722676-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722676
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722676
    reference: chr 8
allele count: 1
allele frequency: 8.394050297149381e-6
allele num: 119132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*80+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.399+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.453+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.366+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*80+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.486+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.353+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.366+33C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*80+33C>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.366+33C>A
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

8-74722696-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722696
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722696
    reference: chr 8
allele count: 2
allele frequency: 1.668251505596984e-5
allele num: 119886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*80+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.399+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.366+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.366+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.486+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.453+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.353+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*80+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*80+13A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.366+13A>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

8-74722709-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722709
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722709
    reference: chr 8
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.366G>C
  hgvsp: ENSP00000473561.1:p.Lys122Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.366G>C
  hgvsp: ENSP00000403764.2:p.Lys122Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.366G>C
  hgvsp: ENSP00000454445.2:p.Lys122Asn
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*80G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.399G>C
  hgvsp: ENSP00000473516.1:p.Lys133Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*80G>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.453G>C
  hgvsp: ENSP00000428813.2:p.Lys151Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.353G>C
  hgvsp: ENSP00000428835.1:p.Lys118Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.486G>C
  hgvsp: ENSP00000397453.3:p.Lys162Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*80G>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys162Asn
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

8-74722750-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722750
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722750
    reference: chr 8
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.325T>A
  hgvsp: ENSP00000473561.1:p.Cys109Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.445T>A
  hgvsp: ENSP00000397453.3:p.Cys149Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*39T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*39T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.312T>A
  hgvsp: ENSP00000428835.1:p.Cys105Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.358T>A
  hgvsp: ENSP00000473516.1:p.Cys120Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.412T>A
  hgvsp: ENSP00000428813.2:p.Cys138Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*39T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.325T>A
  hgvsp: ENSP00000403764.2:p.Cys109Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.325T>A
  hgvsp: ENSP00000454445.2:p.Cys109Ser
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys149Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-74722757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722757
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722757
    reference: chr 8
allele count: 4
allele frequency: 3.315045333244932e-5
allele num: 120662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.305A>G
  hgvsp: ENST00000523278.1:c.305A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.318A>G
  hgvsp: ENST00000602593.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*32A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.318A>G
  hgvsp: ENST00000358757.5:c.318A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.405A>G
  hgvsp: ENST00000517608.1:c.405A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*32A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.438A>G
  hgvsp: ENST00000419880.3:c.438A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.318A>G
  hgvsp: ENST00000453587.2:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*32A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.351A>G
  hgvsp: ENST00000602969.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln146Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

8-74722763-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722763
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722763
    reference: chr 8
allele count: 3
allele frequency: 2.486119167978785e-5
allele num: 120670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.399A>T
  hgvsp: ENST00000517608.1:c.399A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.345A>T
  hgvsp: ENST00000602969.1:c.345A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.312A>T
  hgvsp: ENST00000453587.2:c.312A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*26A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*26A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.312A>T
  hgvsp: ENST00000602593.1:c.312A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.432A>T
  hgvsp: ENST00000419880.3:c.432A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*26A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.312A>T
  hgvsp: ENST00000358757.5:c.312A>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.299A>T
  hgvsp: ENST00000523278.1:c.299A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ser144Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-74722766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722766
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722766
    reference: chr 8
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.342C>T
  hgvsp: ENST00000602969.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.296C>T
  hgvsp: ENST00000523278.1:c.296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.396C>T
  hgvsp: ENST00000517608.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.309C>T
  hgvsp: ENST00000453587.2:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*23C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.429C>T
  hgvsp: ENST00000419880.3:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.309C>T
  hgvsp: ENST00000602593.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.309C>T
  hgvsp: ENST00000358757.5:c.309C>T(p.%3D)
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu143Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

8-74722769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722769
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722769
    reference: chr 8
allele count: 32
allele frequency: 2.651904398846422e-4
allele num: 120668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*20G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*20G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.426G>A
  hgvsp: ENST00000419880.3:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.306G>A
  hgvsp: ENST00000358757.5:c.306G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.306G>A
  hgvsp: ENST00000602593.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.393G>A
  hgvsp: ENST00000517608.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.293G>A
  hgvsp: ENST00000523278.1:c.293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.339G>A
  hgvsp: ENST00000602969.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*20G>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.306G>A
  hgvsp: ENST00000453587.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9963
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala142Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

8-74722775-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722775
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722775
    reference: chr 8
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.300C>G
  hgvsp: ENST00000453587.2:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*14C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*14C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.420C>G
  hgvsp: ENST00000419880.3:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.300C>G
  hgvsp: ENST00000602593.1:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.300C>G
  hgvsp: ENST00000358757.5:c.300C>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.333C>G
  hgvsp: ENST00000602969.1:c.333C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.287C>G
  hgvsp: ENST00000523278.1:c.287C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*14C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.387C>G
  hgvsp: ENST00000517608.1:c.387C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser140Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-74722788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722788
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722788
    reference: chr 8
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.320C>T
  hgvsp: ENSP00000473516.1:p.Thr107Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.274C>T
  hgvsp: ENSP00000428835.1:p.Thr92Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.287C>T
  hgvsp: ENSP00000403764.2:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.407C>T
  hgvsp: ENSP00000397453.3:p.Thr136Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.374C>T
  hgvsp: ENSP00000428813.2:p.Thr125Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.287C>T
  hgvsp: ENSP00000473561.1:p.Thr96Ile
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.*1C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.287C>T
  hgvsp: ENSP00000454445.2:p.Thr96Ile
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.*1C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.*1C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr136Ile
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

8-74722815-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722815
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722815
    reference: chr 8
allele count: 1
allele frequency: 8.306061763875276e-6
allele num: 120394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.157A>G
  hgvsp: ENSP00000430254.1:p.Met53Val
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.260A>G
  hgvsp: ENSP00000454445.2:p.Asn87Ser
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.247A>G
  hgvsp: ENSP00000428835.1:p.Asn83Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.380A>G
  hgvsp: ENSP00000397453.3:p.Asn127Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.260A>G
  hgvsp: ENSP00000403764.2:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.260A>G
  hgvsp: ENSP00000473561.1:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.347A>G
  hgvsp: ENSP00000428813.2:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.157A>G
  hgvsp: ENSP00000429136.1:p.Met53Val
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.293A>G
  hgvsp: ENSP00000473516.1:p.Asn98Ser
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.157A>G
  hgvsp: ENSP00000414771.2:p.Met53Val
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30340
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn87Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/8-74722829-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722829
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722829
    reference: chr 8
allele count: 1
allele frequency: 8.347245409015026e-6
allele num: 119800
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.366T>G
  hgvsp: ENST00000419880.3:c.366T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.279T>G
  hgvsp: ENST00000602969.1:c.279T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.246T>G
  hgvsp: ENST00000602593.1:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.246T>G
  hgvsp: ENST00000358757.5:c.246T>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.143T>G
  hgvsp: ENSP00000429136.1:p.Leu48Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.246T>G
  hgvsp: ENST00000453587.2:c.246T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.333T>G
  hgvsp: ENST00000517608.1:c.333T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.233T>G
  hgvsp: ENST00000523278.1:c.233T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.143T>G
  hgvsp: ENSP00000414771.2:p.Leu48Arg
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.143T>G
  hgvsp: ENSP00000430254.1:p.Leu48Arg
  variant of: http://identifiers.org/hgnc/25616
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu48Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-74722871-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722871
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722871
    reference: chr 8
allele count: 10
allele frequency: 9.393552265724806e-5
allele num: 106456
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.331-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.198-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.211-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.211-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.298-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.211-7C>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.108-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.108-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.108-7C>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.244-7C>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20320
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11157
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.211-7C>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

8-74722872-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722872
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722872
    reference: chr 8
allele count: 2
allele frequency: 1.887647236484446e-5
allele num: 105952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.211-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.298-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.108-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.331-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.198-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.108-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.108-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.244-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.211-8T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.211-8T>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12842
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.211-8T>C
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: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

8-74722906-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74722906
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74722906
    reference: chr 8
allele count: 1
allele frequency: 1.264030741227627e-5
allele num: 79112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.108-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.211-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.298-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.108-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.211-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.211-42T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.108-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.198-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.244-42T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.331-42T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10889
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/8-74737351-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737351
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737352
    reference: chr 8
allele count: 872
allele frequency: 6.635215340130877e-2
allele num: 13142
alternate allele: CA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.330+30dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.210+30dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.210+30dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5264dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5264dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.297+30dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.197+30dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.210+30dupT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.243+30dupT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5264dupT
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 3.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 29109
  bin: 2.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 7.5e0
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 1.75e1
  variant carriers: 356
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.25e1
  variant carriers: 357
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.75e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1304
  bin: 1.25e1
  variant carriers: 99
genotype quality: GenotypeQuality
  all individuals: 13579
  bin: 2.5e0
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 21474
  bin: 7.5e0
  variant carriers: 94
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-74737351-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737351
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737350
    reference: chr 8
allele count: 1307
allele frequency: 9.945213818292498e-2
allele num: 13142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.243+30delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.210+30delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.197+30delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.210+30delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5264delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5264delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.330+30delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.297+30delT
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.210+30delT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5264delT
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29109
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 7.5e0
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 1.75e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.75e1
  variant carriers: 251
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 3.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.25e1
  variant carriers: 352
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 2.25e1
  variant carriers: 94
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 76
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 6.75e1
  variant carriers: 50
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: CA
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

8-74737366-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737366
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737366
    reference: chr 8
allele count: 1
allele frequency: 4.410337831877922e-5
allele num: 22674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.210+16T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.197+16T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.330+16T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.210+16T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5250T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5250T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.243+16T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5250T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.297+16T>A
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.210+16T>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33800
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

8-74737390-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737390
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 23768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.202T>C
  hgvsp: ENSP00000473561.1:p.Ser68Pro
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5226T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.289T>C
  hgvsp: ENSP00000428813.2:p.Ser97Pro
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.202T>C
  hgvsp: ENSP00000454445.2:p.Ser68Pro
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.322T>C
  hgvsp: ENSP00000397453.3:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5226T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5226T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.202T>C
  hgvsp: ENSP00000403764.2:p.Ser68Pro
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.189T>C
  hgvsp: ENSP00000428835.1:p.Ser64Pro
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.235T>C
  hgvsp: ENSP00000473516.1:p.Ser79Pro
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31103
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser108Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP

8-74737427-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737427
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737427
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 25282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.252A>G
  hgvsp: ENST00000517608.1:c.252A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5189A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.152A>G
  hgvsp: ENST00000523278.1:c.152A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.285A>G
  hgvsp: ENST00000419880.3:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5189A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.198A>G
  hgvsp: ENST00000602969.1:c.198A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.165A>G
  hgvsp: ENST00000602593.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.165A>G
  hgvsp: ENST00000358757.5:c.165A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.165A>G
  hgvsp: ENST00000453587.2:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5189A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23020
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln95Gln
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

8-74737433-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737433
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737433
    reference: chr 8
allele count: 1
allele frequency: 3.925262992620505e-5
allele num: 25476
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.279A>T
  hgvsp: ENSP00000397453.3:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.146A>T
  hgvsp: ENSP00000428835.1:p.Lys49Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5183A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5183A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.246A>T
  hgvsp: ENSP00000428813.2:p.Lys82Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.159A>T
  hgvsp: ENSP00000473561.1:p.Lys53Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.159A>T
  hgvsp: ENSP00000403764.2:p.Lys53Asn
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.159A>T
  hgvsp: ENSP00000454445.2:p.Lys53Asn
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5183A>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.192A>T
  hgvsp: ENSP00000473516.1:p.Lys64Asn
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23313
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys93Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-74737434-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737434
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737434
    reference: chr 8
allele count: 1
allele frequency: 3.912363067292644e-5
allele num: 25560
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.245A>C
  hgvsp: ENSP00000428813.2:p.Lys82Thr
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.278A>C
  hgvsp: ENSP00000397453.3:p.Lys93Thr
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5182A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5182A>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.145A>C
  hgvsp: ENSP00000428835.1:p.Lys49Thr
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.191A>C
  hgvsp: ENSP00000473516.1:p.Lys64Thr
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.158A>C
  hgvsp: ENSP00000473561.1:p.Lys53Thr
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.158A>C
  hgvsp: ENSP00000454445.2:p.Lys53Thr
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.158A>C
  hgvsp: ENSP00000403764.2:p.Lys53Thr
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5182A>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys93Thr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

8-74737457-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737457
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737457
    reference: chr 8
allele count: 1
allele frequency: 3.870268596640607e-5
allele num: 25838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.135A>G
  hgvsp: ENST00000602593.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.255A>G
  hgvsp: ENST00000419880.3:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.168A>G
  hgvsp: ENST00000602969.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5159A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.122A>G
  hgvsp: ENST00000523278.1:c.122A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5159A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.135A>G
  hgvsp: ENST00000358757.5:c.135A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5159A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.135A>G
  hgvsp: ENST00000453587.2:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.222A>G
  hgvsp: ENST00000517608.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro85Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

8-74737467-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737467
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737467
    reference: chr 8
allele count: 1
allele frequency: 3.850596842510589e-5
allele num: 25970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.212A>G
  hgvsp: ENSP00000428813.2:p.Glu71Gly
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.245A>G
  hgvsp: ENSP00000397453.3:p.Glu82Gly
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5149A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.125A>G
  hgvsp: ENSP00000454445.2:p.Glu42Gly
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.125A>G
  hgvsp: ENSP00000473561.1:p.Glu42Gly
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.112A>G
  hgvsp: ENSP00000428835.1:p.Glu38Gly
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5149A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5149A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.125A>G
  hgvsp: ENSP00000403764.2:p.Glu42Gly
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.158A>G
  hgvsp: ENSP00000473516.1:p.Glu53Gly
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu82Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum

8-74737488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737488
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737488
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 25088
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.108-4C>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.228-4C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5128C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.141-4C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.108-4C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.195-4C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5128C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.95-4C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.108-4C>T
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5128C>T
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13127
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
hgvs: c.228-4C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

8-74737491-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737491
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737491
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 24938
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.108-7A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.195-7A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5125A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.95-7A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.108-7A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.228-7A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.108-7A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5125A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.141-7A>G
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5125A>G
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12330
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 9.25e1
  variant carriers: 0
hgvs: c.228-7A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

8-74737502-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737502
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737502
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 24010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.195-18T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.108-18T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.108-18T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5114T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.228-18T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.95-18T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5114T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.141-18T>C
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.108-18T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5114T>C
  variant of: http://identifiers.org/hgnc/25616
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33427
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP

8-74737532-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74737532
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 74737533
    reference: chr 8
allele count: 1
allele frequency: 4.574146921599122e-5
allele num: 21862
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428835
  ensembl transcript: ENST00000523278
  gene symbol: UBE2W
  hgvsc: ENST00000523278.1:c.95-49dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473516
  ensembl transcript: ENST00000602969
  gene symbol: UBE2W
  hgvsc: ENST00000602969.1:c.141-49dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000403764
  ensembl transcript: ENST00000453587
  gene symbol: UBE2W
  hgvsc: ENST00000453587.2:c.108-49dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000428813
  ensembl transcript: ENST00000517608
  gene symbol: UBE2W
  hgvsc: ENST00000517608.1:c.195-49dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000430254
  ensembl transcript: ENST00000519277
  gene symbol: UBE2W
  hgvsc: ENST00000519277.1:c.107+5083dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000473561
  ensembl transcript: ENST00000602593
  gene symbol: UBE2W
  hgvsc: ENST00000602593.1:c.108-49dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000429136
  ensembl transcript: ENST00000519255
  gene symbol: UBE2W
  hgvsc: ENST00000519255.1:c.107+5083dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000397453
  ensembl transcript: ENST00000419880
  gene symbol: UBE2W
  hgvsc: ENST00000419880.3:c.228-49dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104343
  ensembl protein: ENSP00000414771
  ensembl transcript: ENST00000422906
  gene symbol: UBE2W
  hgvsc: ENST00000422906.2:c.107+5083dupA
  variant of: http://identifiers.org/hgnc/25616
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258677
  ensembl protein: ENSP00000454445
  ensembl transcript: ENST00000358757
  gene symbol: RP11-463D19.2
  hgvsc: ENST00000358757.5:c.108-49dupA
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22608
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 755
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14116
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4450
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6424
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4544
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.693021365929638e-5
allele num: 59066
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.238e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.033e1

DP
type: SiteQuality
SIO_000300: 1.490949e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e0

FS
type: SiteQuality
SIO_000300: 1.1418e1

VQSLOD
type: SiteQuality
SIO_000300: 5.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

GenotypeQuality
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4618
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4539
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14234
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.704971697469822e-5
allele num: 58652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.593e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 1.460878e6

GenotypeQuality
all individuals: 4974
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6319
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2495
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4541
bin: 9.75e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13946
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.048437827636821e-4
allele num: 57228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7316
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.305483028720627e-3
allele num: 766
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.3e0

FS
type: SiteQuality
SIO_000300: 5.172e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.397053e6

GenotypeQuality
all individuals: 8224
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6667
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1769
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12200
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1103
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4965
bin: 9.75e1
variant carriers: 487

GenotypeQuality
all individuals: 486
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 6329
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2689
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 922
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1825
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1214
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 706
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3251
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 682
bin: 8.25e1
variant carriers: 8

African
type: Population
allele count: 6
allele frequency: 7.309941520467836e-4
allele num: 8208
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.141327623126338e-4
allele num: 9340
num of homozygotes: 0

South Asian
type: Population
allele count: 29
allele frequency: 2.106945655332752e-3
allele num: 13764
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 13
allele frequency: 2.222982216142271e-3
allele num: 5848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 313
allele frequency: 5.542766070479901e-3
allele num: 56470
num of homozygotes: 2

East Asian
type: Population
allele count: 162
allele frequency: 2.245011086474501e-2
allele num: 7216
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.67379679144385e-3
allele num: 748
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.345e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 7.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

DP
type: SiteQuality
SIO_000300: 1.372987e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

GenotypeQuality
all individuals: 1813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8266
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6710
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4918
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12439
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4527
bin: 9.75e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.77695642902836e-5
allele num: 56276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13728
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.19e-1

QD
type: SiteQuality
SIO_000300: 8.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.361e-1

DP
type: SiteQuality
SIO_000300: 1.369492e6

FS
type: SiteQuality
SIO_000300: 3.757e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

GenotypeQuality
all individuals: 2915
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4949
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2319
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8357
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6811
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.388798581350672e-5
allele num: 13534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

DP
type: SiteQuality
SIO_000300: 1.352021e6

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.4e0

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.81910790948119e-5
allele num: 54972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.372e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQ
type: SiteQuality
SIO_000300: 6.054e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

DP
type: SiteQuality
SIO_000300: 1.350126e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.244090569793481e-4
allele num: 8038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54972
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.350126e6

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

QD
type: SiteQuality
SIO_000300: 2.372e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

MQ
type: SiteQuality
SIO_000300: 6.054e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4525
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.122334455667789e-4
allele num: 8910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.346969e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

QD
type: SiteQuality
SIO_000300: 8.050000000000001e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 799
bin: 3.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.112e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.28e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.358000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 1.718e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.05949e5

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2948
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.538461538461538e-3
allele num: 1300
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.121e0

VQSLOD
type: SiteQuality
SIO_000300: -3.618e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.21e-2

DP
type: SiteQuality
SIO_000300: 7.11487e5

QD
type: SiteQuality
SIO_000300: 1.015e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.979e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.52e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.59485e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.927e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.562008469449486e-5
allele num: 13224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.93812e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.04e-2

FS
type: SiteQuality
SIO_000300: 3.299e0

QD
type: SiteQuality
SIO_000300: 2.309e1

VQSLOD
type: SiteQuality
SIO_000300: -2.178e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 494
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13280
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.097560975609756e-4
allele num: 1640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 1.012e1

DP
type: SiteQuality
SIO_000300: 7.97233e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeQuality
all individuals: 1360
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 728
bin: 2.5e0
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GenotypeQuality
all individuals: 816
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.426110203475419e-5
allele num: 13466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.998e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.93e-2

QD
type: SiteQuality
SIO_000300: 1.251e1

DP
type: SiteQuality
SIO_000300: 8.04182e5

GenotypeQuality
all individuals: 501
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7822
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.772314777190844e-5
allele num: 14766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.001e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.26e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.102e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.408e0

DP
type: SiteQuality
SIO_000300: 8.47302e5

GenotypeQuality
all individuals: 7873
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12256
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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: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 1442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14948
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.19e-2

DP
type: SiteQuality
SIO_000300: 8.50356e5

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.567e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 29309
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 6.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1578
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variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 11769
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 507
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variant carriers: 0

GenotypeQuality
all individuals: 394
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variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 163
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variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8138
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.570302233902759e-5
allele num: 15220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.088e-1

QD
type: SiteQuality
SIO_000300: 7.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

FS
type: SiteQuality
SIO_000300: 3.522e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 8.578e5

GenotypeDepth
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
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variant carriers: 0

GenotypeQuality
all individuals: 810
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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: 109
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GenotypeQuality
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GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
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variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8834
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 409
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variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1964
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.589e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

DP
type: SiteQuality
SIO_000300: 8.7763e5

GenotypeDepth
all individuals: 374
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.09979260705136e-5
allele num: 16394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2464
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.23e0

DP
type: SiteQuality
SIO_000300: 8.81667e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.44069640914037e-5
allele num: 18380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1516
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.532e0

QD
type: SiteQuality
SIO_000300: 8.07e0

VQSLOD
type: SiteQuality
SIO_000300: -3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 3.976e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.65e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 9.19214e5

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 109
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GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 166
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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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Latino
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European (Finnish)
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.575961336415213e-4
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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European (Non-Finnish)
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allele num: 19096
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Other
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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DP
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 6.038647342995169e-4
allele num: 1656
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DP
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MQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 4.5662100456621e-4
allele num: 2190
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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SIO_000300: -2.08e-2

ReadPosRankSum
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SIO_000300: -1.398e0

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

Latino
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allele frequency: 0.0e0
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African
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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VQSLOD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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Other
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European (Finnish)
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Latino
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East Asian
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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FS
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.518e1

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2613
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5126
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23883
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 9.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.22e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.068e-1

DP
type: SiteQuality
SIO_000300: 7.60443e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 3408
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25301
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2689
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.941176470588235e-4
allele num: 3400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1934
num of homozygotes: 0

Latino
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: 1878
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

FS
type: SiteQuality
SIO_000300: 2.049e0

DP
type: SiteQuality
SIO_000300: 7.36454e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.58e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e-1

QD
type: SiteQuality
SIO_000300: 1.585e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

GenotypeQuality
all individuals: 3399
bin: 1.25e1
variant carriers: 23

GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 24

GenotypeQuality
all individuals: 11792
bin: 2.25e1
variant carriers: 53

GenotypeQuality
all individuals: 1206
bin: 6.75e1
variant carriers: 26

GenotypeQuality
all individuals: 25066
bin: 7.5e0
variant carriers: 26

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 20

GenotypeQuality
all individuals: 3228
bin: 9.75e1
variant carriers: 609

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 38

GenotypeQuality
all individuals: 456
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1791
bin: 1.75e1
variant carriers: 41

GenotypeQuality
all individuals: 2098
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 30

GenotypeQuality
all individuals: 487
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 189
bin: 4.75e1
variant carriers: 18

GenotypeQuality
all individuals: 926
bin: 2.75e1
variant carriers: 41

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 41

GenotypeQuality
all individuals: 817
bin: 3.25e1
variant carriers: 18

Other
type: Population
allele count: 4
allele frequency: 1.324503311258278e-2
allele num: 302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 6.376195536663124e-3
allele num: 1882
num of homozygotes: 0

East Asian
type: Population
allele count: 366
allele frequency: 1.799410029498525e-1
allele num: 2034
num of homozygotes: 25

African
type: Population
allele count: 3
allele frequency: 8.917954815695601e-4
allele num: 3364
num of homozygotes: 0

South Asian
type: Population
allele count: 132
allele frequency: 1.560283687943262e-2
allele num: 8460
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 4.36871996505024e-4
allele num: 13734
num of homozygotes: 0

Latino
type: Population
allele count: 34
allele frequency: 3.78619153674833e-2
allele num: 898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.34722e5

QD
type: SiteQuality
SIO_000300: 1.674e1

VQSLOD
type: SiteQuality
SIO_000300: 5.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 3190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7290
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25165
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5136
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.25689404934688e-4
allele num: 1378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12202
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

QD
type: SiteQuality
SIO_000300: 1.639e1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.92686e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.11e-2

GenotypeQuality
all individuals: 615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6562
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24673
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.350033400133601e-5
allele num: 11976
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1754
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 6.90564e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.25e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

FS
type: SiteQuality
SIO_000300: 2.308e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 7.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.568e-1

GenotypeQuality
all individuals: 935
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6562
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5331
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1348
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 2.308e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.25e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 7.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 6.90564e5

VQSLOD
type: SiteQuality
SIO_000300: -1.568e-1

GenotypeQuality
all individuals: 5404
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3886
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24347
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4482
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1332
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.684919966301601e-4
allele num: 11870
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.35e-2

DP
type: SiteQuality
SIO_000300: 6.89731e5

QD
type: SiteQuality
SIO_000300: 3.038e1

VQSLOD
type: SiteQuality
SIO_000300: -1.93e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2665
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5462
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4441
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5516
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2673
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 462
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1294
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.506311360448808e-4
allele num: 2852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.45e-2

QD
type: SiteQuality
SIO_000300: 1.649e1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

DP
type: SiteQuality
SIO_000300: 6.88377e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1290
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11776
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1738
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2854
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.48e-2

QD
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SIO_000300: 9.67e0

DP
type: SiteQuality
SIO_000300: 6.88398e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1238
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2786
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1730
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: 0.0e0

DP
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SIO_000300: 6.87302e5

FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -5.5e-1

BaseQRankSum
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SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.61e-2

QD
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SIO_000300: 8.18e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 5.894836123555765e-4
allele num: 8482
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65574
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.632366e6

FS
type: SiteQuality
SIO_000300: 9.18e0

QD
type: SiteQuality
SIO_000300: 1.176e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.497e1

MQRankSum
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SIO_000300: -1.872e0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.218917601170161e-4
allele num: 65632
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.972e0

QD
type: SiteQuality
SIO_000300: 1.312e1

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

FS
type: SiteQuality
SIO_000300: 1.241e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 1.639209e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65720
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.077e0

DP
type: SiteQuality
SIO_000300: 1.643672e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.14e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

FS
type: SiteQuality
SIO_000300: 1.1972e1

BaseQRankSum
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SIO_000300: -1.911e0

QD
type: SiteQuality
SIO_000300: 1.579e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66192
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

BaseQRankSum
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DP
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SIO_000300: 1.658289e6

ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 9.236000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

Other
type: Population
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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

East Asian
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.000390050706592e-5
allele num: 66658
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 2.44e0

FS
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.228e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000030000300003e-5
allele num: 66666
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: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.218e0

DP
type: SiteQuality
SIO_000300: 1.6682e6

QD
type: SiteQuality
SIO_000300: 1.205e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45636
bin: 6.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.23e0

QD
type: SiteQuality
SIO_000300: 1.479e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.536e0

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

DP
type: SiteQuality
SIO_000300: 1.668247e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
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variant carriers: 1

GenotypeQuality
all individuals: 4
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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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.975e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.84e-1

DP
type: SiteQuality
SIO_000300: 1.668205e6

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.35e-1

FS
type: SiteQuality
SIO_000300: 7.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.81e-1

QD
type: SiteQuality
SIO_000300: 1.039e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 221
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variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 9.75e1
variant carriers: 32

GenotypeQuality
all individuals: 1667
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.7997600119994e-4
allele num: 66670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

DP
type: SiteQuality
SIO_000300: 1.669859e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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: 0

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1669
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

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: 9794
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.667939e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.586e0

QD
type: SiteQuality
SIO_000300: 1.046e1

FS
type: SiteQuality
SIO_000300: 4.276e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.225e0

GenotypeQuality
all individuals: 45632
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

DP
type: SiteQuality
SIO_000300: 1.667743e6

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.630000000000001e-2

QD
type: SiteQuality
SIO_000300: 8.18e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1654
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.143e-1

DP
type: SiteQuality
SIO_000300: 1.665751e6

MQRankSum
type: SiteQuality
SIO_000300: -1.061e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.47e1

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
all individuals: 517
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
all individuals: 1669
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GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 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: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66190
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.000000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.894e0

MQ
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SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.654813e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 10

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.696525515743757e-4
allele num: 58944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.331294e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

FS
type: SiteQuality
SIO_000300: 3.311e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.409245874812491e-5
allele num: 58664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14064
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.314339e6

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

QD
type: SiteQuality
SIO_000300: 8.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.95e-1

FS
type: SiteQuality
SIO_000300: 2.036e0

VQSLOD
type: SiteQuality
SIO_000300: -7.066e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3405
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.373e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

QD
type: SiteQuality
SIO_000300: 7.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.36508e5

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 53

GenotypeQuality
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variant carriers: 87

GenotypeQuality
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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: 65

GenotypeQuality
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variant carriers: 96

GenotypeQuality
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variant carriers: 113

GenotypeQuality
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GenotypeQuality
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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: 16

GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 198
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variant carriers: 17

East Asian
type: Population
allele count: 15
allele frequency: 3.36322869955157e-2
allele num: 446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 204
allele frequency: 3.308465780084333e-2
allele num: 6166
num of homozygotes: 0

South Asian
type: Population
allele count: 564
allele frequency: 1.940812112869924e-1
allele num: 2906
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 4.166666666666666e-2
allele num: 288
num of homozygotes: 0

African
type: Population
allele count: 62
allele frequency: 3.677342823250297e-2
allele num: 1686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 2.013422818791947e-3
allele num: 1490
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 7.5e-2
allele num: 160
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.56758e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.890000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

GenotypeQuality
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variant carriers: 79

GenotypeQuality
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GenotypeQuality
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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: 25

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 71

African
type: Population
allele count: 64
allele frequency: 3.795966785290629e-2
allele num: 1686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 670
allele frequency: 1.086603957184561e-1
allele num: 6166
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 6.944444444444445e-2
allele num: 288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.711409395973154e-4
allele num: 1490
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 7.5e-2
allele num: 160
num of homozygotes: 0

South Asian
type: Population
allele count: 489
allele frequency: 1.682725395732966e-1
allele num: 2906
num of homozygotes: 0

East Asian
type: Population
allele count: 51
allele frequency: 1.143497757847534e-1
allele num: 446
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

DP
type: SiteQuality
SIO_000300: 4.56758e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.890000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.336513443191674e-4
allele num: 2306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.7604e5

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.54e-2

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1024
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GenotypeQuality
all individuals: 164
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 8.99e0

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.836e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.86e-1

FS
type: SiteQuality
SIO_000300: 5.722e0

DP
type: SiteQuality
SIO_000300: 5.44931e5

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

South Asian
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African
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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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allele frequency: 0.0e0
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Latino
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ReadPosRankSum
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VQSLOD
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 11298
num of homozygotes: 0

Latino
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Other
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African
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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ReadPosRankSum
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SIO_000300: -3.86e-1

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

South Asian
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allele num: 8006
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African
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East Asian
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European (Non-Finnish)
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Other
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Latino
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.41e-1

QD
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 8.656509695290859e-5
allele num: 11552
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Other
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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Other
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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South Asian
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.1115e5

GenotypeQuality
all individuals: 1760
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 7.75e1
variant carriers: 0