5-50055451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055451
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055451
    reference: chr 5
allele count: 1
allele frequency: 8.952872081363702e-6
allele num: 111696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2204A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2204A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-26A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18452A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

5-50055456-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055457
    reference: chr 5
allele count: 9871
allele frequency: 2.930297452947812e-1
allele num: 33686
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2183dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2183dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18431dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-5dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-5dupT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 1.25e1
  variant carriers: 2237
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 428
genotype quality: GenotypeQuality
num of homozygotes: 1865
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

5-50055456-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055458
    reference: chr 5
allele count: 7575
allele frequency: 2.248708662352313e-1
allele num: 33686
alternate allele: CTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-6_281-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2184_367-2183dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-6_130-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2184_367-2183dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18432_147-18431dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-6_272-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-6_-557-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-6_*6-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-6_*89-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-6_147-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-6_185-5dupTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-6_122-5dupTT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 68
genotype quality: GenotypeQuality
num of homozygotes: 1161
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

5-50055456-C-CTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055459
    reference: chr 5
allele count: 1703
allele frequency: 5.055512675889094e-2
allele num: 33686
alternate allele: CTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-7_281-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2185_367-2183dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-7_*6-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18433_147-18431dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-7_147-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-7_-557-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-7_130-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-7_185-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-7_122-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-7_272-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2185_367-2183dupTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-7_*89-5dupTTT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 251
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-50055456-C-CTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055460
    reference: chr 5
allele count: 309
allele frequency: 9.172950187021314e-3
allele num: 33686
alternate allele: CTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-8_-557-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-8_130-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-8_*89-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-8_147-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-8_122-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18434_147-18431dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-8_272-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2186_367-2183dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-8_281-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2186_367-2183dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-8_185-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-8_*6-5dupTTTT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 53
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

5-50055456-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055455
    reference: chr 5
allele count: 2891
allele frequency: 8.582200320607968e-2
allele num: 33686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2183delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2183delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18431delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-5delT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: CT
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

5-50055456-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055454
    reference: chr 5
allele count: 383
allele frequency: 1.136970848423677e-2
allele num: 33686
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 2.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 1.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 6.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 2.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 24360
  bin: 2.5e0
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 2.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 3.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 1.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 4.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 5.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 6.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 7.5e0
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 5.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.25e1
  variant carriers: 12
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 7
  allele frequency: 2.592592592592593e-3
  allele num: 2700
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 37
  allele frequency: 1.76022835394862e-2
  allele num: 2102
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 19
  allele frequency: 1.162790697674419e-2
  allele num: 1634
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 176
  allele frequency: 8.137599408174588e-3
  allele num: 21628
  num of homozygotes: 0
population: African
population: South Asian
population: Other
reference allele: CTT
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-50055467-T-TTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055467
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055469
    reference: chr 5
allele count: 1
allele frequency: 9.8405825624877e-6
allele num: 101620
alternate allele: TTA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-9_130-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-9_*89-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-9_147-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-9_272-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-9_281-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2187_367-2186insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-9_-557-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18435_147-18434insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-9_122-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2187_367-2186insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-9_185-8insAT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-9_*6-8insAT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

5-50055468-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055468
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055468
    reference: chr 5
allele count: 1
allele frequency: 9.261831990367695e-6
allele num: 107970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18435T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2187T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2187T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-9T>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

5-50055472-T-TTTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055472
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055475
    reference: chr 5
allele count: 1
allele frequency: 8.482627578718784e-6
allele num: 117888
alternate allele: TTTC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-5_-557-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2183_367-2182insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-5_272-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-5_130-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-5_122-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-5_281-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18431_147-18430insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-5_147-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-5_*6-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-5_*89-4insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2183_367-2182insTTC
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-5_185-4insTTC
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.185-5_185-4insTTC
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

5-50055473-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055473
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055473
    reference: chr 5
allele count: 46
allele frequency: 2.927325951380934e-3
allele num: 15714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2182G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18430G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2182G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-4G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-4G>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.185-4G>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

5-50055473-GCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055473
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055471
    reference: chr 5
allele count: 1
allele frequency: 6.363752068219422e-5
allele num: 15714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-557-3_-557-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.147-3_147-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*6-3_*6-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*89-3_*89-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.122-3_122-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.281-3_281-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.272-3_272-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2181_367-2180delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.185-3_185-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2181_367-2180delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.130-3_130-2delCA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18429_147-18428delCA
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.185-3_185-2delCA
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: GCA
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

5-50055484-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055484
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055484
    reference: chr 5
allele count: 1
allele frequency: 8.427439743805831e-6
allele num: 118660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.192A>G
  hgvsp: ENST00000514067.2:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-550A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.192A>G
  hgvsp: ENST00000515166.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.137A>G
  hgvsp: ENSP00000424916.1:p.His46Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*96A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2171A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.192A>G
  hgvsp: ENST00000505697.2:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*13A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.288A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18419A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*4A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.192A>G
  hgvsp: ENST00000503707.2:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.192A>G
  hgvsp: ENST00000281631.5:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.192A>G
  hgvsp: ENST00000502524.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.192A>G
  hgvsp: ENST00000503046.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.192A>G
  hgvsp: ENST00000503750.2:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.129A>G
  hgvsp: ENST00000505554.1:c.129A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.279A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2171A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His46Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

5-50055488-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055488
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055488
    reference: chr 5
allele count: 1
allele frequency: 8.40463263350759e-6
allele num: 118982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.133G>C
  hgvsp: ENSP00000423946.1:p.Val45Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.196G>C
  hgvsp: ENSP00000422217.2:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*8G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2167G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*100G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.283G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.141G>C
  hgvsp: ENSP00000424916.1:p.Met47Ile
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.196G>C
  hgvsp: ENSP00000281631.4:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*17G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-546G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18415G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.196G>C
  hgvsp: ENSP00000421708.1:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2167G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.196G>C
  hgvsp: ENSP00000426243.1:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.196G>C
  hgvsp: ENSP00000440851.1:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.196G>C
  hgvsp: ENSP00000424814.2:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.292G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.196G>C
  hgvsp: ENSP00000426679.2:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.196G>C
  hgvsp: ENSP00000424485.1:p.Val66Leu
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val66Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-50055490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055490
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055490
    reference: chr 5
allele count: 10
allele frequency: 8.386306838194596e-5
allele num: 119242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.143G>A
  hgvsp: ENSP00000424916.1:p.Cys48Tyr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.198G>A
  hgvsp: ENST00000514067.2:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.198G>A
  hgvsp: ENST00000503707.2:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2165G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.198G>A
  hgvsp: ENST00000515166.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.198G>A
  hgvsp: ENST00000505697.2:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-544G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2165G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.294G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*10G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.135G>A
  hgvsp: ENST00000505554.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.198G>A
  hgvsp: ENST00000503046.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.198G>A
  hgvsp: ENST00000503750.2:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.285G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.198G>A
  hgvsp: ENST00000281631.5:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18413G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*19G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.198G>A
  hgvsp: ENST00000502524.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys48Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

5-50055490-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055490
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055490
    reference: chr 5
allele count: 1
allele frequency: 8.386306838194597e-6
allele num: 119242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*19G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.198G>T
  hgvsp: ENST00000503707.2:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.198G>T
  hgvsp: ENST00000514067.2:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.198G>T
  hgvsp: ENST00000502524.1:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*102G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-544G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.294G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.143G>T
  hgvsp: ENSP00000424916.1:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.198G>T
  hgvsp: ENST00000515166.1:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.198G>T
  hgvsp: ENST00000505697.2:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.198G>T
  hgvsp: ENST00000281631.5:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2165G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2165G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.198G>T
  hgvsp: ENST00000503750.2:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.285G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.135G>T
  hgvsp: ENST00000505554.1:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*10G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.198G>T
  hgvsp: ENST00000503046.1:c.198G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18413G>T
  variant of: http://identifiers.org/hgnc/26124
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys48Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

5-50055495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055495
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055495
    reference: chr 5
allele count: 3
allele frequency: 2.504382669671926e-5
allele num: 119790
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.203G>A
  hgvsp: ENSP00000281631.4:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.140G>A
  hgvsp: ENSP00000423946.1:p.Ser47Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2160G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.203G>A
  hgvsp: ENSP00000422217.2:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-539G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.203G>A
  hgvsp: ENSP00000440851.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.203G>A
  hgvsp: ENSP00000424814.2:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.148G>A
  hgvsp: ENSP00000424916.1:p.Val50Ile
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.203G>A
  hgvsp: ENSP00000426679.2:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.203G>A
  hgvsp: ENSP00000426243.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.203G>A
  hgvsp: ENSP00000421708.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.203G>A
  hgvsp: ENSP00000424485.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18408G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2160G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.290G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.299G>A
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser68Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-50055495-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055495
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055495
    reference: chr 5
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.203G>C
  hgvsp: ENSP00000426679.2:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*24G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.203G>C
  hgvsp: ENSP00000424485.1:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.203G>C
  hgvsp: ENSP00000422217.2:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.140G>C
  hgvsp: ENSP00000423946.1:p.Ser47Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.203G>C
  hgvsp: ENSP00000281631.4:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2160G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.148G>C
  hgvsp: ENSP00000424916.1:p.Val50Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.203G>C
  hgvsp: ENSP00000426243.1:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.290G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18408G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-539G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.203G>C
  hgvsp: ENSP00000424814.2:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2160G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.299G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.203G>C
  hgvsp: ENSP00000421708.1:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*107G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*15G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.203G>C
  hgvsp: ENSP00000440851.1:p.Ser68Thr
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser68Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

5-50055502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055502
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055502
    reference: chr 5
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.210G>A
  hgvsp: ENST00000502524.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.210G>A
  hgvsp: ENST00000281631.5:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.155G>A
  hgvsp: ENSP00000424916.1:p.Arg52Lys
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.210G>A
  hgvsp: ENST00000514067.2:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18401G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-532G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*31G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.210G>A
  hgvsp: ENST00000515166.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.210G>A
  hgvsp: ENST00000503046.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.147G>A
  hgvsp: ENST00000505554.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.297G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.210G>A
  hgvsp: ENST00000503750.2:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.210G>A
  hgvsp: ENST00000505697.2:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.306G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.210G>A
  hgvsp: ENST00000503707.2:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2153G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2153G>A
  variant of: http://identifiers.org/hgnc/26124
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg52Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-50055503-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055503
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055503
    reference: chr 5
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.148A>G
  hgvsp: ENSP00000423946.1:p.Asn50Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.211A>G
  hgvsp: ENSP00000281631.4:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-531A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.211A>G
  hgvsp: ENSP00000426679.2:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.156A>G
  hgvsp: ENST00000503193.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.211A>G
  hgvsp: ENSP00000424485.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18400A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.307A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*115A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.211A>G
  hgvsp: ENSP00000421708.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.211A>G
  hgvsp: ENSP00000424814.2:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.298A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.211A>G
  hgvsp: ENSP00000422217.2:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.211A>G
  hgvsp: ENSP00000440851.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2152A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.211A>G
  hgvsp: ENSP00000426243.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2152A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*23A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn71Asp
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-50055504-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055504
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055504
    reference: chr 5
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.212A>C
  hgvsp: ENSP00000440851.1:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.212A>C
  hgvsp: ENSP00000421708.1:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.212A>C
  hgvsp: ENSP00000424814.2:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*24A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.212A>C
  hgvsp: ENSP00000281631.4:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.308A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.299A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.212A>C
  hgvsp: ENSP00000424485.1:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.212A>C
  hgvsp: ENSP00000426679.2:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.212A>C
  hgvsp: ENSP00000426243.1:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-530A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.149A>C
  hgvsp: ENSP00000423946.1:p.Asn50Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.212A>C
  hgvsp: ENSP00000422217.2:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.157A>C
  hgvsp: ENSP00000424916.1:p.Met53Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2151A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*33A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*116A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2151A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18399A>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn71Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

5-50055517-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055517
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055517
    reference: chr 5
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18386G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.225G>T
  hgvsp: ENST00000505697.2:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.225G>T
  hgvsp: ENST00000503046.1:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.162G>T
  hgvsp: ENST00000505554.1:c.162G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.321G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*46G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.225G>T
  hgvsp: ENST00000514067.2:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.170G>T
  hgvsp: ENSP00000424916.1:p.Cys57Phe
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-517G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.225G>T
  hgvsp: ENST00000503707.2:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.225G>T
  hgvsp: ENST00000281631.5:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.225G>T
  hgvsp: ENST00000515166.1:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.225G>T
  hgvsp: ENST00000503750.2:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.312G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2138G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*37G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.225G>T
  hgvsp: ENST00000502524.1:c.225G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*129G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2138G>T
  variant of: http://identifiers.org/hgnc/26124
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys57Phe
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD

5-50055521-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055521
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055521
    reference: chr 5
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-513G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.166G>C
  hgvsp: ENSP00000423946.1:p.Val56Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.229G>C
  hgvsp: ENSP00000424814.2:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.325G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2134G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426243
  ensembl transcript: ENST00000502524
  gene symbol: PARP8
  hgvsc: ENST00000502524.1:c.229G>C
  hgvsp: ENSP00000426243.1:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2134G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*133G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.229G>C
  hgvsp: ENSP00000426679.2:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.229G>C
  hgvsp: ENSP00000424485.1:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.229G>C
  hgvsp: ENSP00000440851.1:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.316G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.174G>C
  hgvsp: ENSP00000424916.1:p.Ter58TyrextTer8
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.229G>C
  hgvsp: ENSP00000421708.1:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.229G>C
  hgvsp: ENSP00000281631.4:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.229G>C
  hgvsp: ENSP00000422217.2:p.Val77Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18382G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*50G>C
  variant of: http://identifiers.org/hgnc/26124
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ter58TyrextTer8
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

5-50055526-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055526
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055526
    reference: chr 5
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.234T>G
  hgvsp: ENST00000514067.2:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.234T>G
  hgvsp: ENST00000503046.1:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.171T>G
  hgvsp: ENST00000505554.1:c.171T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.234T>G
  hgvsp: ENST00000515166.1:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.321T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*138T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.234T>G
  hgvsp: ENST00000503707.2:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.234T>G
  hgvsp: ENST00000505697.2:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-508T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.234T>G
  hgvsp: ENST00000281631.5:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2129T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*5T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.330T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.234T>G
  hgvsp: ENST00000503750.2:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18377T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*55T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*46T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2129T>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr78Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/5-50055529-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055529
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055529
    reference: chr 5
allele count: 1
allele frequency: 8.283768783445716e-6
allele num: 120718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-505A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.174A>C
  hgvsp: ENST00000505554.1:c.174A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*141A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.333A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18374A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.237A>C
  hgvsp: ENST00000505697.2:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.237A>C
  hgvsp: ENST00000503046.1:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.237A>C
  hgvsp: ENST00000281631.5:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*49A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.237A>C
  hgvsp: ENST00000514067.2:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*8A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*58A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.237A>C
  hgvsp: ENST00000503750.2:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.324A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.237A>C
  hgvsp: ENST00000503707.2:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2126A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2126A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.237A>C
  hgvsp: ENST00000515166.1:c.237A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr79Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

5-50055540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055540
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055540
    reference: chr 5
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.248C>T
  hgvsp: ENSP00000422217.2:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.344C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.248C>T
  hgvsp: ENSP00000424814.2:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.248C>T
  hgvsp: ENSP00000281631.4:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.185C>T
  hgvsp: ENSP00000423946.1:p.Pro62Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*152C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*69C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.248C>T
  hgvsp: ENSP00000424485.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2115C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.248C>T
  hgvsp: ENSP00000421708.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*19C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.335C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-494C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.248C>T
  hgvsp: ENSP00000440851.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18363C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.248C>T
  hgvsp: ENSP00000426679.2:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2115C>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro83Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

5-50055550-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055550
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055550
    reference: chr 5
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*162T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.258T>C
  hgvsp: ENST00000505697.2:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.258T>C
  hgvsp: ENST00000503707.2:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.258T>C
  hgvsp: ENST00000281631.5:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.345T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2105T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18353T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.354T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.258T>C
  hgvsp: ENST00000514067.2:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.258T>C
  hgvsp: ENST00000503046.1:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-484T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*29T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.195T>C
  hgvsp: ENST00000505554.1:c.195T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.258T>C
  hgvsp: ENST00000515166.1:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*79T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.258T>C
  hgvsp: ENST00000503750.2:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*70T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2105T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe86Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

5-50055553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055553
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055553
    reference: chr 5
allele count: 4
allele frequency: 3.318785988085559e-5
allele num: 120526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.261T>C
  hgvsp: ENST00000505697.2:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.261T>C
  hgvsp: ENST00000515166.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.261T>C
  hgvsp: ENST00000503750.2:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*82T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.261T>C
  hgvsp: ENST00000503046.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-481T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.261T>C
  hgvsp: ENST00000503707.2:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18350T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.261T>C
  hgvsp: ENST00000514067.2:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.261T>C
  hgvsp: ENST00000281631.5:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.357T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*73T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*165T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2102T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.198T>C
  hgvsp: ENST00000505554.1:c.198T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2102T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*32T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.348T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His87His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

5-50055556-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055556
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055556
    reference: chr 5
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.351A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.264A>G
  hgvsp: ENST00000281631.5:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*76A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.264A>G
  hgvsp: ENST00000514067.2:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*35A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.360A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18347A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.264A>G
  hgvsp: ENST00000505697.2:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.264A>G
  hgvsp: ENST00000503707.2:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*85A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.264A>G
  hgvsp: ENST00000515166.1:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.201A>G
  hgvsp: ENST00000505554.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.264A>G
  hgvsp: ENST00000503750.2:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2099A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2099A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*168A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-478A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.264A>G
  hgvsp: ENST00000503046.1:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg88Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/5-50055557-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055557
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055557
    reference: chr 5
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.361A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*169A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.265A>C
  hgvsp: ENSP00000422217.2:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-477A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.265A>C
  hgvsp: ENSP00000440851.1:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.265A>C
  hgvsp: ENSP00000281631.4:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.265A>C
  hgvsp: ENSP00000421708.1:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.265A>C
  hgvsp: ENSP00000426679.2:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.265A>C
  hgvsp: ENSP00000424485.1:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.265A>C
  hgvsp: ENSP00000424814.2:p.Ile89Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.202A>C
  hgvsp: ENSP00000423946.1:p.Ile68Leu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18346A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*36A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*86A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2098A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.352A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2098A>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*77A>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20544
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile89Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

5-50055570-ATAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055570
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055567
    reference: chr 5
allele count: 1
allele frequency: 8.367220576668843e-6
allele num: 119514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+10_*45+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+10_370+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+10_211+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2079_367-2077delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2079_367-2077delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+10_361+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+10_*178+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+10_*95+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+10_274+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+10_*86+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+10_-468+12delGTA
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18327_147-18325delGTA
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.274+10_274+12delGTA
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: ATAG
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

5-50055579-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055579
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055579
    reference: chr 5
allele count: 37
allele frequency: 3.138359231865373e-4
allele num: 117896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2076T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+13T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2076T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18324T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+13T>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

5-50055581-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055581
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055580
    reference: chr 5
allele count: 2
allele frequency: 1.700362177143732e-5
allele num: 117622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2068delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2068delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+21delT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18316delT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: AT
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

5-50055588-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055588
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055588
    reference: chr 5
allele count: 1
allele frequency: 8.637368711995577e-6
allele num: 115776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18315A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2067A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2067A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+22A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

5-50055589-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055589
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055589
    reference: chr 5
allele count: 3
allele frequency: 2.591210613598673e-5
allele num: 115776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2066T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2066T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18314T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+23T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+23T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

5-50055596-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055596
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055596
    reference: chr 5
allele count: 1
allele frequency: 8.807468733485996e-6
allele num: 113540
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2059T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2059T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18307T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+30T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+30T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

5-50055599-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055599
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055600
    reference: chr 5
allele count: 1
allele frequency: 8.872642095363157e-6
allele num: 112706
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2050dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18298dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2050dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+39dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+39dupT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-50055613-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055613
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055613
    reference: chr 5
allele count: 1
allele frequency: 9.277126317351936e-6
allele num: 107792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18290A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2042A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+47A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2042A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+47A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

5-50055614-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055614
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055614
    reference: chr 5
allele count: 5
allele frequency: 4.71902901259037e-5
allele num: 105954
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18289T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2041T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2041T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+48T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+48T>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

5-50055616-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50055616
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50055616
    reference: chr 5
allele count: 1
allele frequency: 9.428447511832702e-6
allele num: 106062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.211+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*95+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-2039A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*178+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*86+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-468+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*45+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-2039A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.370+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-18287A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.274+50A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-50056083-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056083
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056083
    reference: chr 5
allele count: 1
allele frequency: 1.940315883425822e-5
allele num: 51538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.275-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+517T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.212-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1572T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17820T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+517T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-467-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.275-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*179-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.275-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*46-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.275-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*96-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.275-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.275-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.371-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*87-43T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1572T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

5-50056093-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056093
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056093
    reference: chr 5
allele count: 1
allele frequency: 1.894800666969835e-5
allele num: 52776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1562C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*96-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+527C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.275-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17810C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-467-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*179-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.275-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+527C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.275-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*46-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.275-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.275-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.212-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.275-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1562C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.371-33C>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*87-33C>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-50056096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056096
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056096
    reference: chr 5
allele count: 4
allele frequency: 7.475517679599313e-5
allele num: 53508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1559A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.275-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+530A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*179-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.212-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*96-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-467-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.275-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.275-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+530A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17807A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.275-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*46-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1559A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.275-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*87-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.275-30A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.371-30A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

5-50056101-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056101
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056101
    reference: chr 5
allele count: 3
allele frequency: 5.526693931690063e-5
allele num: 54282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*179-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.275-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+535T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.275-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*46-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+535T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*87-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1554T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.275-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.371-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.275-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.212-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.275-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-467-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1554T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*96-25T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17802T>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.275-25T>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7984
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-50056146-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056146
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056146
    reference: chr 5
allele count: 4
allele frequency: 4.430954649179166e-5
allele num: 90274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.391A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17757A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1509A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*199A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.232A>G
  hgvsp: ENSP00000423946.1:p.Ile78Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.295A>G
  hgvsp: ENSP00000424485.1:p.Ile99Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+580A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.295A>G
  hgvsp: ENSP00000422217.2:p.Ile99Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.295A>G
  hgvsp: ENSP00000440851.1:p.Ile99Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.295A>G
  hgvsp: ENSP00000424814.2:p.Ile99Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*116A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.295A>G
  hgvsp: ENSP00000421708.1:p.Ile99Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.295A>G
  hgvsp: ENSP00000281631.4:p.Ile99Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+580A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*66A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-447A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1509A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile99Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

5-50056155-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056155
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056155
    reference: chr 5
allele count: 1
allele frequency: 1.058716412221822e-5
allele num: 94454
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17748T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+589T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-438T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.304T>C
  hgvsp: ENSP00000422217.2:p.Cys102Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.304T>C
  hgvsp: ENSP00000281631.4:p.Cys102Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.304T>C
  hgvsp: ENSP00000424814.2:p.Cys102Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.400T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.304T>C
  hgvsp: ENSP00000421708.1:p.Cys102Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*208T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1500T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*116T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1500T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*125T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.241T>C
  hgvsp: ENSP00000423946.1:p.Cys81Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+589T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.304T>C
  hgvsp: ENSP00000440851.1:p.Cys102Arg
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*75T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.304T>C
  hgvsp: ENSP00000424485.1:p.Cys102Arg
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys102Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

5-50056170-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056170
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056170
    reference: chr 5
allele count: 1
allele frequency: 1.033314044804497e-5
allele num: 96776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*90T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+604T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-423T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*131T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.319T>A
  hgvsp: ENSP00000440851.1:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1485T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.319T>A
  hgvsp: ENSP00000422217.2:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.319T>A
  hgvsp: ENSP00000424485.1:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*223T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.319T>A
  hgvsp: ENSP00000421708.1:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.319T>A
  hgvsp: ENSP00000424814.2:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+604T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17733T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*140T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.415T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1485T>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.319T>A
  hgvsp: ENSP00000281631.4:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.256T>A
  hgvsp: ENSP00000423946.1:p.Ser86Thr
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser107Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/5-50056172-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056172
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056172
    reference: chr 5
allele count: 1
allele frequency: 1.03511096389533e-5
allele num: 96608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.417C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.321C>A
  hgvsp: ENST00000503750.2:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*142C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*225C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.321C>A
  hgvsp: ENST00000514067.2:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.321C>A
  hgvsp: ENST00000505697.2:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*92C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+606C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*133C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17731C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1483C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.321C>A
  hgvsp: ENST00000515166.1:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.321C>A
  hgvsp: ENST00000281631.5:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.258C>A
  hgvsp: ENST00000505554.1:c.258C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.321C>A
  hgvsp: ENST00000503046.1:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+606C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-421C>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1483C>A
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser107Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

5-50056181-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056181
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056181
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 95890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-412A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.330A>T
  hgvsp: ENSP00000440851.1:p.Gln110His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*151A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.330A>T
  hgvsp: ENSP00000424485.1:p.Gln110His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1474A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.426A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.267A>T
  hgvsp: ENSP00000423946.1:p.Gln89His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.330A>T
  hgvsp: ENSP00000421708.1:p.Gln110His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*142A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.330A>T
  hgvsp: ENSP00000281631.4:p.Gln110His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+615A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.330A>T
  hgvsp: ENSP00000422217.2:p.Gln110His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*101A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.330A>T
  hgvsp: ENSP00000424814.2:p.Gln110His
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*234A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1474A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+615A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17722A>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 34143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln110His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

5-50056182-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056182
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056182
    reference: chr 5
allele count: 1
allele frequency: 1.045019437361535e-5
allele num: 95692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*152A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*235A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*143A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.268A>G
  hgvsp: ENSP00000423946.1:p.Lys90Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.331A>G
  hgvsp: ENSP00000422217.2:p.Lys111Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+616A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.331A>G
  hgvsp: ENSP00000440851.1:p.Lys111Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1473A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.331A>G
  hgvsp: ENSP00000424485.1:p.Lys111Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.331A>G
  hgvsp: ENSP00000424814.2:p.Lys111Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.427A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.331A>G
  hgvsp: ENSP00000421708.1:p.Lys111Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-411A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17721A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1473A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+616A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.331A>G
  hgvsp: ENSP00000281631.4:p.Lys111Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*102A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys111Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

5-50056191-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056191
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056191
    reference: chr 5
allele count: 1
allele frequency: 1.086295298513948e-5
allele num: 92056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.277G>T
  hgvsp: ENSP00000423946.1:p.Gly93Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+625G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.340G>T
  hgvsp: ENSP00000421708.1:p.Gly114Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.340G>T
  hgvsp: ENSP00000440851.1:p.Gly114Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.340G>T
  hgvsp: ENSP00000422217.2:p.Gly114Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1464G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*111G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.340G>T
  hgvsp: ENSP00000281631.4:p.Gly114Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+625G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.340G>T
  hgvsp: ENSP00000424814.2:p.Gly114Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1464G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17712G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*161G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-402G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.436G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.340G>T
  hgvsp: ENSP00000424485.1:p.Gly114Trp
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*152G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*244G>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly114Trp
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

5-50056192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056192
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056192
    reference: chr 5
allele count: 1
allele frequency: 1.086106525328004e-5
allele num: 92072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-401G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+626G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*153G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.437G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.341G>A
  hgvsp: ENSP00000421708.1:p.Gly114Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.341G>A
  hgvsp: ENSP00000422217.2:p.Gly114Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+626G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*112G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.341G>A
  hgvsp: ENSP00000440851.1:p.Gly114Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17711G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.278G>A
  hgvsp: ENSP00000423946.1:p.Gly93Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.341G>A
  hgvsp: ENSP00000281631.4:p.Gly114Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1463G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*245G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*162G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1463G>A
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.341G>A
  hgvsp: ENSP00000424814.2:p.Gly114Glu
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.341G>A
  hgvsp: ENSP00000424485.1:p.Gly114Glu
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly114Glu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum

5-50056192-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056192
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056192
    reference: chr 5
allele count: 12
allele frequency: 1.303327830393605e-4
allele num: 92072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1463G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.341G>T
  hgvsp: ENSP00000440851.1:p.Gly114Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.341G>T
  hgvsp: ENSP00000421708.1:p.Gly114Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.341G>T
  hgvsp: ENSP00000281631.4:p.Gly114Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.341G>T
  hgvsp: ENSP00000424814.2:p.Gly114Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.341G>T
  hgvsp: ENSP00000422217.2:p.Gly114Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+626G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17711G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.341G>T
  hgvsp: ENSP00000424485.1:p.Gly114Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.437G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+626G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.278G>T
  hgvsp: ENSP00000423946.1:p.Gly93Val
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-401G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*112G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*153G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*162G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1463G>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*245G>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly114Val
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

5-50056200-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056200
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056200
    reference: chr 5
allele count: 1
allele frequency: 1.143432125869008e-5
allele num: 87456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+634T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421708
  ensembl transcript: ENST00000503046
  gene symbol: PARP8
  hgvsc: ENST00000503046.1:c.349T>C
  hgvsp: ENST00000503046.1:c.349T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17703T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1455T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+634T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+4T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1455T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.345+4T>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

5-50056205-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056205
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056205
    reference: chr 5
allele count: 1
allele frequency: 1.182676159613975e-5
allele num: 84554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1450A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+639A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17698A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+639A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+9A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1450A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+9A>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

5-50056206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056206
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056206
    reference: chr 5
allele count: 1
allele frequency: 1.224319890300938e-5
allele num: 81678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1449T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+640T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17697T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1449T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+640T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+10T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+10T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

5-50056208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056208
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056208
    reference: chr 5
allele count: 1
allele frequency: 1.223062058168832e-5
allele num: 81762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+642A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+642A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17695A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1447A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+12A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1447A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+12A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

5-50056208-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056208
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056208
    reference: chr 5
allele count: 1
allele frequency: 1.223062058168832e-5
allele num: 81762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+642A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1447A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+642A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17695A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+12A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1447A>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

5-50056210-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056210
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056211
    reference: chr 5
allele count: 1
allele frequency: 1.261320350142529e-5
allele num: 79282
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1439dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+650dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+650dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17687dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1439dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+20dupT
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+20dupT
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

5-50056213-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056213
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056213
    reference: chr 5
allele count: 2
allele frequency: 2.607222004953722e-5
allele num: 76710
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+647T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+647T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17690T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+17T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1442T>C
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1442T>C
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-50056228-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056228
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056228
    reference: chr 5
allele count: 1
allele frequency: 1.60040970488445e-5
allele num: 62484
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1427A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+662A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1427A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+662A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+32A>G
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17675A>G
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11979
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

5-50056230-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50056230
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 50056230
    reference: chr 5
allele count: 1
allele frequency: 1.654642928056125e-5
allele num: 60436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423946
  ensembl transcript: ENST00000505554
  gene symbol: PARP8
  hgvsc: ENST00000505554.1:c.282+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000505180
  gene symbol: PARP8
  hgvsc: ENST00000505180.1:n.441+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000511363
  gene symbol: PARP8
  hgvsc: ENST00000511363.2:n.367-1425A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000421503
  ensembl transcript: ENST00000503888
  gene symbol: PARP8
  hgvsc: ENST00000503888.1:c.*249+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000281631
  ensembl transcript: ENST00000281631
  gene symbol: PARP8
  hgvsc: ENST00000281631.5:c.345+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424485
  ensembl transcript: ENST00000515166
  gene symbol: PARP8
  hgvsc: ENST00000515166.1:c.345+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503561
  gene symbol: PARP8
  hgvsc: ENST00000503561.3:n.361+664A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000423133
  ensembl transcript: ENST00000515175
  gene symbol: PARP8
  hgvsc: ENST00000515175.1:c.147-17673A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000439022
  ensembl transcript: ENST00000514342
  gene symbol: PARP8
  hgvsc: ENST00000514342.2:c.-397+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422183
  ensembl transcript: ENST00000507812
  gene symbol: PARP8
  hgvsc: ENST00000507812.1:c.*157+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422217
  ensembl transcript: ENST00000505697
  gene symbol: PARP8
  hgvsc: ENST00000505697.2:c.345+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424814
  ensembl transcript: ENST00000514067
  gene symbol: PARP8
  hgvsc: ENST00000514067.2:c.345+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000424916
  ensembl transcript: ENST00000503193
  gene symbol: PARP8
  hgvsc: ENST00000503193.1:c.*116+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000440851
  ensembl transcript: ENST00000503750
  gene symbol: PARP8
  hgvsc: ENST00000503750.2:c.345+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000426679
  ensembl transcript: ENST00000503707
  gene symbol: PARP8
  hgvsc: ENST00000503707.2:c.274+664A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl protein: ENSP00000422288
  ensembl transcript: ENST00000510303
  gene symbol: PARP8
  hgvsc: ENST00000510303.2:c.*166+34A>T
  variant of: http://identifiers.org/hgnc/26124
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151883
  ensembl transcript: ENST00000503790
  gene symbol: PARP8
  hgvsc: ENST00000503790.2:n.367-1425A>T
  variant of: http://identifiers.org/hgnc/26124
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19302
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 12561
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7209
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 327
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 458
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3276
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 435
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5588
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19847
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1626
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3105
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 814
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 587
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4791
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2404
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5680
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21508
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.261670451678022e-4
allele num: 7926
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.025e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

DP
type: SiteQuality
SIO_000300: 1.60824e6

MQ
type: SiteQuality
SIO_000300: 5.617e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 8.57e0

GenotypeDepth
all individuals: 1793
bin: 7.5e0
variant carriers: 771

GenotypeDepth
all individuals: 926
bin: 5.75e1
variant carriers: 110

GenotypeDepth
all individuals: 131
bin: 7.75e1
variant carriers: 42

GenotypeDepth
all individuals: 189
bin: 7.25e1
variant carriers: 44

GenotypeDepth
all individuals: 7374
bin: 1.75e1
variant carriers: 2786

GenotypeDepth
all individuals: 7174
bin: 2.25e1
variant carriers: 1946

GenotypeDepth
all individuals: 322
bin: 6.75e1
variant carriers: 66

GenotypeDepth
all individuals: 3049
bin: 4.25e1
variant carriers: 300

GenotypeDepth
all individuals: 266
bin: 2.5e0
variant carriers: 77

GenotypeDepth
all individuals: 6405
bin: 2.75e1
variant carriers: 1151

GenotypeDepth
all individuals: 551
bin: 6.25e1
variant carriers: 67

GenotypeDepth
all individuals: 2339
bin: 4.75e1
variant carriers: 194

GenotypeDepth
all individuals: 65
bin: 9.25e1
variant carriers: 25

GenotypeDepth
all individuals: 305
bin: 9.75e1
variant carriers: 120

GenotypeDepth
all individuals: 1555
bin: 5.25e1
variant carriers: 125

GenotypeDepth
all individuals: 5140
bin: 3.25e1
variant carriers: 658

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 21

GenotypeDepth
all individuals: 90
bin: 8.25e1
variant carriers: 29

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 239

GenotypeQuality
all individuals: 24360
bin: 2.5e0
variant carriers: 697

GenotypeQuality
all individuals: 1344
bin: 3.75e1
variant carriers: 615

GenotypeQuality
all individuals: 1267
bin: 4.25e1
variant carriers: 609

GenotypeQuality
all individuals: 1057
bin: 5.25e1
variant carriers: 519

GenotypeQuality
all individuals: 786
bin: 6.25e1
variant carriers: 389

GenotypeQuality
all individuals: 1748
bin: 7.5e0
variant carriers: 707

GenotypeQuality
all individuals: 1485
bin: 1.25e1
variant carriers: 663

GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 210

GenotypeQuality
all individuals: 3740
bin: 9.75e1
variant carriers: 1845

GenotypeQuality
all individuals: 624
bin: 7.25e1
variant carriers: 312

GenotypeQuality
all individuals: 1598
bin: 2.25e1
variant carriers: 667

GenotypeQuality
all individuals: 540
bin: 7.75e1
variant carriers: 275

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 649

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 659

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 548

GenotypeQuality
all individuals: 667
bin: 6.75e1
variant carriers: 320

GenotypeQuality
all individuals: 875
bin: 5.75e1
variant carriers: 437

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 215

GenotypeQuality
all individuals: 1360
bin: 2.75e1
variant carriers: 622

East Asian
type: Population
allele count: 504
allele frequency: 3.084455324357405e-1
allele num: 1634
num of homozygotes: 183

South Asian
type: Population
allele count: 428
allele frequency: 1.682389937106918e-1
allele num: 2544
num of homozygotes: 124

Latino
type: Population
allele count: 678
allele frequency: 3.225499524262607e-1
allele num: 2102
num of homozygotes: 253

European (Finnish)
type: Population
allele count: 989
allele frequency: 3.662962962962963e-1
allele num: 2700
num of homozygotes: 116

African
type: Population
allele count: 878
allele frequency: 3.142448103078024e-1
allele num: 2794
num of homozygotes: 131

Other
type: Population
allele count: 97
allele frequency: 3.415492957746479e-1
allele num: 284
num of homozygotes: 17

European (Non-Finnish)
type: Population
allele count: 6297
allele frequency: 2.911503606436102e-1
allele num: 21628
num of homozygotes: 1041

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.577e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

DP
type: SiteQuality
SIO_000300: 1.811733e6

GenotypeDepth
all individuals: 7374
bin: 1.75e1
variant carriers: 2058

GenotypeDepth
all individuals: 266
bin: 2.5e0
variant carriers: 30

GenotypeDepth
all individuals: 5002
bin: 1.25e1
variant carriers: 1715

GenotypeDepth
all individuals: 6405
bin: 2.75e1
variant carriers: 855

GenotypeDepth
all individuals: 305
bin: 9.75e1
variant carriers: 96

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 28

GenotypeDepth
all individuals: 5140
bin: 3.25e1
variant carriers: 589

GenotypeDepth
all individuals: 322
bin: 6.75e1
variant carriers: 51

GenotypeDepth
all individuals: 2339
bin: 4.75e1
variant carriers: 203

GenotypeDepth
all individuals: 3049
bin: 4.25e1
variant carriers: 268

GenotypeDepth
all individuals: 7174
bin: 2.25e1
variant carriers: 1364

GenotypeDepth
all individuals: 4030
bin: 3.75e1
variant carriers: 356

GenotypeDepth
all individuals: 90
bin: 8.25e1
variant carriers: 40

GenotypeDepth
all individuals: 131
bin: 7.75e1
variant carriers: 39

GenotypeDepth
all individuals: 189
bin: 7.25e1
variant carriers: 40

GenotypeDepth
all individuals: 926
bin: 5.75e1
variant carriers: 105

GenotypeDepth
all individuals: 1793
bin: 7.5e0
variant carriers: 588

GenotypeDepth
all individuals: 65
bin: 9.25e1
variant carriers: 26

GenotypeQuality
all individuals: 875
bin: 5.75e1
variant carriers: 322

GenotypeQuality
all individuals: 3740
bin: 9.75e1
variant carriers: 1861

GenotypeQuality
all individuals: 1267
bin: 4.25e1
variant carriers: 433

GenotypeQuality
all individuals: 1057
bin: 5.25e1
variant carriers: 358

GenotypeQuality
all individuals: 667
bin: 6.75e1
variant carriers: 226

GenotypeQuality
all individuals: 1485
bin: 1.25e1
variant carriers: 477

GenotypeQuality
all individuals: 1598
bin: 2.25e1
variant carriers: 486

GenotypeQuality
all individuals: 1344
bin: 3.75e1
variant carriers: 442

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 400

GenotypeQuality
all individuals: 1748
bin: 7.5e0
variant carriers: 472

GenotypeQuality
all individuals: 786
bin: 6.25e1
variant carriers: 290

GenotypeQuality
all individuals: 1360
bin: 2.75e1
variant carriers: 412

GenotypeQuality
all individuals: 24360
bin: 2.5e0
variant carriers: 462

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 434

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 179

GenotypeQuality
all individuals: 540
bin: 7.75e1
variant carriers: 232

GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 206

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 207

GenotypeQuality
all individuals: 624
bin: 7.25e1
variant carriers: 267

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 487

Other
type: Population
allele count: 63
allele frequency: 2.21830985915493e-1
allele num: 284
num of homozygotes: 8

European (Non-Finnish)
type: Population
allele count: 5351
allele frequency: 2.474107638246717e-1
allele num: 21628
num of homozygotes: 716

African
type: Population
allele count: 429
allele frequency: 1.535433070866142e-1
allele num: 2794
num of homozygotes: 59

Latino
type: Population
allele count: 366
allele frequency: 1.741198858230257e-1
allele num: 2102
num of homozygotes: 109

East Asian
type: Population
allele count: 375
allele frequency: 2.294981640146879e-1
allele num: 1634
num of homozygotes: 113

European (Finnish)
type: Population
allele count: 677
allele frequency: 2.507407407407408e-1
allele num: 2700
num of homozygotes: 69

South Asian
type: Population
allele count: 314
allele frequency: 1.234276729559748e-1
allele num: 2544
num of homozygotes: 87

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.577e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

DP
type: SiteQuality
SIO_000300: 1.811733e6

GenotypeDepth
all individuals: 5002
bin: 1.25e1
variant carriers: 469

GenotypeDepth
all individuals: 1793
bin: 7.5e0
variant carriers: 186

GenotypeDepth
all individuals: 3049
bin: 4.25e1
variant carriers: 38

GenotypeDepth
all individuals: 7374
bin: 1.75e1
variant carriers: 558

GenotypeDepth
all individuals: 2339
bin: 4.75e1
variant carriers: 32

GenotypeDepth
all individuals: 926
bin: 5.75e1
variant carriers: 21

GenotypeDepth
all individuals: 4030
bin: 3.75e1
variant carriers: 62

GenotypeDepth
all individuals: 7174
bin: 2.25e1
variant carriers: 324

GenotypeDepth
all individuals: 266
bin: 2.5e0
variant carriers: 7

GenotypeDepth
all individuals: 6405
bin: 2.75e1
variant carriers: 220

GenotypeDepth
all individuals: 305
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 65
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 131
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1555
bin: 5.25e1
variant carriers: 26

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 6.75e1
variant carriers: 8

GenotypeDepth
all individuals: 90
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5140
bin: 3.25e1
variant carriers: 126

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 49

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 107

GenotypeQuality
all individuals: 875
bin: 5.75e1
variant carriers: 81

GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 46

GenotypeQuality
all individuals: 1485
bin: 1.25e1
variant carriers: 120

GenotypeQuality
all individuals: 786
bin: 6.25e1
variant carriers: 60

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 131

GenotypeQuality
all individuals: 1748
bin: 7.5e0
variant carriers: 144

GenotypeQuality
all individuals: 1360
bin: 2.75e1
variant carriers: 104

GenotypeQuality
all individuals: 24360
bin: 2.5e0
variant carriers: 144

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 46

GenotypeQuality
all individuals: 667
bin: 6.75e1
variant carriers: 78

GenotypeQuality
all individuals: 3740
bin: 9.75e1
variant carriers: 394

GenotypeQuality
all individuals: 1598
bin: 2.25e1
variant carriers: 131

GenotypeQuality
all individuals: 1344
bin: 3.75e1
variant carriers: 127

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 77

GenotypeQuality
all individuals: 540
bin: 7.75e1
variant carriers: 50

GenotypeQuality
all individuals: 624
bin: 7.25e1
variant carriers: 43

GenotypeQuality
all individuals: 1057
bin: 5.25e1
variant carriers: 94

GenotypeQuality
all individuals: 1267
bin: 4.25e1
variant carriers: 81

European (Finnish)
type: Population
allele count: 118
allele frequency: 4.37037037037037e-2
allele num: 2700
num of homozygotes: 18

South Asian
type: Population
allele count: 103
allele frequency: 4.04874213836478e-2
allele num: 2544
num of homozygotes: 24

Latino
type: Population
allele count: 80
allele frequency: 3.805899143672693e-2
allele num: 2102
num of homozygotes: 22

African
type: Population
allele count: 88
allele frequency: 3.149606299212598e-2
allele num: 2794
num of homozygotes: 13

East Asian
type: Population
allele count: 94
allele frequency: 5.752753977968176e-2
allele num: 1634
num of homozygotes: 23

European (Non-Finnish)
type: Population
allele count: 1202
allele frequency: 5.557610504901054e-2
allele num: 21628
num of homozygotes: 147

Other
type: Population
allele count: 18
allele frequency: 6.338028169014084e-2
allele num: 284
num of homozygotes: 4

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.577e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

DP
type: SiteQuality
SIO_000300: 1.811733e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

GenotypeDepth
all individuals: 266
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4030
bin: 3.75e1
variant carriers: 16

GenotypeDepth
all individuals: 6405
bin: 2.75e1
variant carriers: 28

GenotypeDepth
all individuals: 926
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5140
bin: 3.25e1
variant carriers: 23

GenotypeDepth
all individuals: 7174
bin: 2.25e1
variant carriers: 48

GenotypeDepth
all individuals: 551
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 131
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7374
bin: 1.75e1
variant carriers: 104

GenotypeDepth
all individuals: 5002
bin: 1.25e1
variant carriers: 88

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1793
bin: 7.5e0
variant carriers: 34

GenotypeDepth
all individuals: 189
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 65
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 90
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2339
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3740
bin: 9.75e1
variant carriers: 73

GenotypeQuality
all individuals: 1485
bin: 1.25e1
variant carriers: 21

GenotypeQuality
all individuals: 1478
bin: 3.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1360
bin: 2.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1748
bin: 7.5e0
variant carriers: 17

GenotypeQuality
all individuals: 1344
bin: 3.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1598
bin: 2.25e1
variant carriers: 19

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 21

GenotypeQuality
all individuals: 1057
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 540
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 24360
bin: 2.5e0
variant carriers: 20

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
all individuals: 432
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variant carriers: 12

GenotypeQuality
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bin: 6.75e1
variant carriers: 9

Other
type: Population
allele count: 2
allele frequency: 7.042253521126761e-3
allele num: 284
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 1.189343482397716e-2
allele num: 2102
num of homozygotes: 8

African
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allele count: 17
allele frequency: 6.084466714387974e-3
allele num: 2794
num of homozygotes: 2

East Asian
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allele count: 15
allele frequency: 9.179926560587515e-3
allele num: 1634
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 196
allele frequency: 9.062326613648974e-3
allele num: 21628
num of homozygotes: 23

South Asian
type: Population
allele count: 34
allele frequency: 1.336477987421384e-2
allele num: 2544
num of homozygotes: 11

European (Finnish)
type: Population
allele count: 20
allele frequency: 7.407407407407408e-3
allele num: 2700
num of homozygotes: 5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

ReadPosRankSum
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SIO_000300: -3.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.577e-1

BaseQRankSum
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SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.921e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 9.460000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

DP
type: SiteQuality
SIO_000300: 1.811733e6

GenotypeDepth
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bin: 2.5e0
variant carriers: 1

GenotypeDepth
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variant carriers: 57

GenotypeDepth
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variant carriers: 74

GenotypeDepth
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variant carriers: 13

GenotypeDepth
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variant carriers: 17

GenotypeDepth
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GenotypeDepth
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variant carriers: 637

GenotypeDepth
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variant carriers: 83

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 957

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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variant carriers: 461

GenotypeDepth
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variant carriers: 1021

GenotypeDepth
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variant carriers: 14

GenotypeDepth
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variant carriers: 28

GenotypeDepth
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variant carriers: 39

GenotypeDepth
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variant carriers: 39

GenotypeQuality
all individuals: 875
bin: 5.75e1
variant carriers: 172

GenotypeQuality
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variant carriers: 187

GenotypeQuality
all individuals: 1267
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variant carriers: 262

GenotypeQuality
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bin: 2.75e1
variant carriers: 311

GenotypeQuality
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variant carriers: 323

GenotypeQuality
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variant carriers: 216

GenotypeQuality
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GenotypeQuality
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variant carriers: 278

GenotypeQuality
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GenotypeQuality
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variant carriers: 275

GenotypeQuality
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variant carriers: 319

GenotypeQuality
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variant carriers: 265

GenotypeQuality
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variant carriers: 66

GenotypeQuality
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variant carriers: 147

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 301

GenotypeQuality
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variant carriers: 66

GenotypeQuality
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bin: 5.25e1
variant carriers: 216

East Asian
type: Population
allele count: 158
allele frequency: 9.669522643818849e-2
allele num: 1634
num of homozygotes: 0

African
type: Population
allele count: 265
allele frequency: 9.484609878310665e-2
allele num: 2794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 126
allele frequency: 4.666666666666667e-2
allele num: 2700
num of homozygotes: 0

South Asian
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allele count: 449
allele frequency: 1.764937106918239e-1
allele num: 2544
num of homozygotes: 0

Latino
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allele count: 219
allele frequency: 1.0418648905804e-1
allele num: 2102
num of homozygotes: 0

Other
type: Population
allele count: 13
allele frequency: 4.577464788732395e-2
allele num: 284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1661
allele frequency: 7.679859441464768e-2
allele num: 21628
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

InbreedingCoeff
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SIO_000300: 6.577e-1

MQ
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SIO_000300: 5.921e1

ReadPosRankSum
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SIO_000300: -3.03e-1

MQRankSum
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SIO_000300: 3.52e-1

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.811733e6

ClippingRankSum
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SIO_000300: 7.65e-1

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

African
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allele count: 34
allele frequency: 1.216893342877595e-2
allele num: 2794
num of homozygotes: 0

South Asian
type: Population
allele count: 107
allele frequency: 4.205974842767295e-2
allele num: 2544
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.056338028169014e-2
allele num: 284
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.921e1

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

DP
type: SiteQuality
SIO_000300: 1.811733e6

MQRankSum
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SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.577e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

GenotypeDepth
all individuals: 392
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variant carriers: 0

GenotypeDepth
all individuals: 6359
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 192
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.772421127259837e-5
allele num: 56420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.178e-1

QD
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SIO_000300: 2.428e1

FS
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SIO_000300: 8.048e0

ClippingRankSum
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SIO_000300: -3.429e0

MQ
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SIO_000300: 6.086e1

BaseQRankSum
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SIO_000300: 8.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 2.42277e6

GenotypeDepth
all individuals: 286
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.122082585278277e-4
allele num: 8912
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
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SIO_000300: -2.923e0

InbreedingCoeff
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SIO_000300: -8.9e-3

ClippingRankSum
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SIO_000300: -1.127e0

BaseQRankSum
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SIO_000300: 1.2e-1

MQ
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FS
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DP
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MQRankSum
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SIO_000300: -5.03e-1

ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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allele frequency: 1.167133520074697e-4
allele num: 8568
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.2433e1

MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 6

GenotypeDepth
all individuals: 167
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
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allele count: 6
allele frequency: 3.141361256544503e-3
allele num: 1910
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.074688796680498e-3
allele num: 964
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.861042183622829e-3
allele num: 1612
num of homozygotes: 0

European (Finnish)
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allele count: 16
allele frequency: 1.82648401826484e-2
allele num: 876
num of homozygotes: 0

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

Latino
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allele count: 5
allele frequency: 6.613756613756613e-3
allele num: 756
num of homozygotes: 0

European (Non-Finnish)
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allele count: 14
allele frequency: 1.475237091675448e-3
allele num: 9490
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.885e-1

ClippingRankSum
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FS
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.787e1

QD
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.037344398340249e-3
allele num: 964
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -1.073e0

FS
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SIO_000300: 5.6536e1

ReadPosRankSum
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SIO_000300: 7.62e-1

InbreedingCoeff
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MQ
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QD
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VQSLOD
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SIO_000300: -1.444e0

MQRankSum
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SIO_000300: -4.23e-1

DP
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SIO_000300: 1.828722e6

BaseQRankSum
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SIO_000300: -1.98e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65364
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
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
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 9.26e-1

QD
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VQSLOD
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SIO_000300: -1.882e-1

InbreedingCoeff
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DP
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SIO_000300: 1.721467e6

BaseQRankSum
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SIO_000300: -1.445e0

ReadPosRankSum
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SIO_000300: -3.85e-1

MQ
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SIO_000300: 6.027e1

ClippingRankSum
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SIO_000300: 5.22e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 1.013376570733685e-4
allele num: 9868
num of homozygotes: 0

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

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

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

European (Finnish)
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allele count: 0
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VQSLOD
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FS
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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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

African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 10
allele frequency: 1.522440777053773e-4
allele num: 65684
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QD
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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VQSLOD
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MQ
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European (Finnish)
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DP
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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VQSLOD
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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MQ
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Latino
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African
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East Asian
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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South Asian
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Latino
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MQRankSum
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DP
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MQ
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QD
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FS
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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South Asian
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FS
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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GenotypeQuality
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East Asian
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Latino
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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African
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East Asian
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Other
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 6.02918123718799e-5
allele num: 66344
num of homozygotes: 0

Latino
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ClippingRankSum
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SIO_000300: -2.26e-1

MQRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66294
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Other
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European (Finnish)
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African
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South Asian
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Latino
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East Asian
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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ReadPosRankSum
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FS
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QD
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VQSLOD
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MQ
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DP
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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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Other
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 1.522394421946838e-5
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num of homozygotes: 0

African
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Latino
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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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num of homozygotes: 0

QD
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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SIO_000300: 3.15e-1

DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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Latino
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African
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allele frequency: 4.105090311986864e-4
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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: 7.733473566987348e-5
allele num: 64654
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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South Asian
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allele num: 16330
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MQ
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SIO_000300: 6.072e1

MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.688616e6

ReadPosRankSum
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SIO_000300: -4.61e-1

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

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

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

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

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

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

MQRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 26254
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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South Asian
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East Asian
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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DP
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 9746
num of homozygotes: 0

East Asian
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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European (Finnish)
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MQ
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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allele frequency: 1.007861318282604e-4
allele num: 9922
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.955569461827284e-5
allele num: 51136
num of homozygotes: 0

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

African
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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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ClippingRankSum
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SIO_000300: -1.39e-1

VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 9.71e-1

DP
type: SiteQuality
SIO_000300: 1.23634e6

QD
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SIO_000300: 9.08e0

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

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

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

European (Non-Finnish)
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allele num: 51080
num of homozygotes: 0

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

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

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

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

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

Latino
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allele frequency: 0.0e0
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Other
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MQRankSum
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SIO_000300: -7.29e-1

VQSLOD
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BaseQRankSum
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FS
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DP
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QD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -4.4e-3

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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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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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele num: 50526
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Other
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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MQ
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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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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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
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European (Finnish)
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.374759417102007e-4
allele num: 7274
num of homozygotes: 0

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

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

African
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num of homozygotes: 0

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 (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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SIO_000300: 3.074e0

ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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