8-145060340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060340
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060340
    reference: chr 8
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.64G>A
  hgvsp: ENSP00000435161.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.64G>A
  hgvsp: ENSP00000436333.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.100G>A
  hgvsp: ENSP00000434776.1:p.Val34Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.64G>A
  hgvsp: ENSP00000325618.7:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.64G>A
  hgvsp: ENSP00000314320.5:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.64G>A
  hgvsp: ENSP00000436301.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.64G>A
  hgvsp: ENSP00000434411.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.64G>A
  hgvsp: ENSP00000436697.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.64G>A
  hgvsp: ENSP00000433990.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.64G>A
  hgvsp: ENSP00000432733.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.64G>A
  hgvsp: ENSP00000431620.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.64G>A
  hgvsp: ENSP00000431818.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.64G>A
  hgvsp: ENSP00000432204.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.165G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.64G>A
  hgvsp: ENSP00000435793.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.64G>A
  hgvsp: ENSP00000431250.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.64G>A
  hgvsp: ENSP00000434005.1:p.Val22Met
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+186G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val22Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/8-145060340-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060340
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060340
    reference: chr 8
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+186G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.64G>T
  hgvsp: ENSP00000431250.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.64G>T
  hgvsp: ENSP00000436697.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.64G>T
  hgvsp: ENSP00000435161.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.64G>T
  hgvsp: ENSP00000436301.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.64G>T
  hgvsp: ENSP00000431620.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.64G>T
  hgvsp: ENSP00000431818.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.64G>T
  hgvsp: ENSP00000436333.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.64G>T
  hgvsp: ENSP00000434005.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.64G>T
  hgvsp: ENSP00000434411.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.64G>T
  hgvsp: ENSP00000432204.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.64G>T
  hgvsp: ENSP00000325618.7:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.64G>T
  hgvsp: ENSP00000435793.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.64G>T
  hgvsp: ENSP00000432733.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.64G>T
  hgvsp: ENSP00000433990.1:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.64G>T
  hgvsp: ENSP00000314320.5:p.Val22Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.100G>T
  hgvsp: ENSP00000434776.1:p.Val34Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.165G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7521
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val22Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

8-145060341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060341
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060341
    reference: chr 8
allele count: 3
allele frequency: 2.496214075319099e-5
allele num: 120182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.63C>T
  hgvsp: ENST00000528914.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.63C>T
  hgvsp: ENST00000532311.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.63C>T
  hgvsp: ENST00000531707.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.63C>T
  hgvsp: ENST00000529842.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.164C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.63C>T
  hgvsp: ENST00000529311.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.63C>T
  hgvsp: ENST00000313028.7:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.63C>T
  hgvsp: ENST00000524918.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+185C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.63C>T
  hgvsp: ENST00000525486.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.63C>T
  hgvsp: ENST00000527262.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.63C>T
  hgvsp: ENST00000530478.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.63C>T
  hgvsp: ENST00000525879.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.63C>T
  hgvsp: ENST00000313059.5:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.63C>T
  hgvsp: ENST00000531537.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.63C>T
  hgvsp: ENST00000528625.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.99C>T
  hgvsp: ENST00000525773.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.63C>T
  hgvsp: ENST00000528136.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala21Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

8-145060343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060343
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060343
    reference: chr 8
allele count: 1
allele frequency: 8.318083513558476e-6
allele num: 120220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.61G>A
  hgvsp: ENSP00000432204.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.61G>A
  hgvsp: ENSP00000436333.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.61G>A
  hgvsp: ENSP00000325618.7:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.61G>A
  hgvsp: ENSP00000436301.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.162G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.97G>A
  hgvsp: ENSP00000434776.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.61G>A
  hgvsp: ENSP00000434005.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.61G>A
  hgvsp: ENSP00000431250.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.61G>A
  hgvsp: ENSP00000434411.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.61G>A
  hgvsp: ENSP00000431818.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.61G>A
  hgvsp: ENSP00000314320.5:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.61G>A
  hgvsp: ENSP00000433990.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.61G>A
  hgvsp: ENSP00000436697.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.61G>A
  hgvsp: ENSP00000432733.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.61G>A
  hgvsp: ENSP00000435793.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+183G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.61G>A
  hgvsp: ENSP00000431620.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.61G>A
  hgvsp: ENSP00000435161.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala21Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

8-145060357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060357
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060357
    reference: chr 8
allele count: 1
allele frequency: 8.333888925928395e-6
allele num: 119992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.47G>A
  hgvsp: ENSP00000431818.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.47G>A
  hgvsp: ENSP00000433990.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.47G>A
  hgvsp: ENSP00000436301.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+169G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.47G>A
  hgvsp: ENSP00000436333.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.83G>A
  hgvsp: ENSP00000434776.1:p.Arg28His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.47G>A
  hgvsp: ENSP00000434411.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.47G>A
  hgvsp: ENSP00000314320.5:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.47G>A
  hgvsp: ENSP00000436697.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.47G>A
  hgvsp: ENSP00000431620.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.47G>A
  hgvsp: ENSP00000434005.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.47G>A
  hgvsp: ENSP00000435161.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.47G>A
  hgvsp: ENSP00000432733.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.47G>A
  hgvsp: ENSP00000325618.7:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.47G>A
  hgvsp: ENSP00000432204.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.47G>A
  hgvsp: ENSP00000435793.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.148G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.47G>A
  hgvsp: ENSP00000431250.1:p.Arg16His
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg16His
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-145060358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060358
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060358
    reference: chr 8
allele count: 2
allele frequency: 1.666139055965611e-5
allele num: 120038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.46C>T
  hgvsp: ENSP00000434411.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.46C>T
  hgvsp: ENSP00000325618.7:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.46C>T
  hgvsp: ENSP00000431250.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.46C>T
  hgvsp: ENSP00000431620.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.46C>T
  hgvsp: ENSP00000436697.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.46C>T
  hgvsp: ENSP00000434005.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.46C>T
  hgvsp: ENSP00000435793.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.46C>T
  hgvsp: ENSP00000432204.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.46C>T
  hgvsp: ENSP00000436301.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.46C>T
  hgvsp: ENSP00000436333.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.46C>T
  hgvsp: ENSP00000432733.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.46C>T
  hgvsp: ENSP00000431818.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.82C>T
  hgvsp: ENSP00000434776.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.46C>T
  hgvsp: ENSP00000435161.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.46C>T
  hgvsp: ENSP00000433990.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.46C>T
  hgvsp: ENSP00000314320.5:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.147C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+168C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg16Cys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-145060361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060361
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060361
    reference: chr 8
allele count: 2
allele frequency: 1.665223472990075e-5
allele num: 120104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.43G>A
  hgvsp: ENSP00000432733.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.43G>A
  hgvsp: ENSP00000435793.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.43G>A
  hgvsp: ENSP00000436333.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.43G>A
  hgvsp: ENSP00000436301.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.43G>A
  hgvsp: ENSP00000434005.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.43G>A
  hgvsp: ENSP00000325618.7:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.43G>A
  hgvsp: ENSP00000431620.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.79G>A
  hgvsp: ENSP00000434776.1:p.Val27Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.144G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.43G>A
  hgvsp: ENSP00000436697.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+165G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.43G>A
  hgvsp: ENSP00000434411.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.43G>A
  hgvsp: ENSP00000432204.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.43G>A
  hgvsp: ENSP00000431250.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.43G>A
  hgvsp: ENSP00000435161.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.43G>A
  hgvsp: ENSP00000431818.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.43G>A
  hgvsp: ENSP00000314320.5:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.43G>A
  hgvsp: ENSP00000433990.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val15Ile
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

8-145060371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060371
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060371
    reference: chr 8
allele count: 1
allele frequency: 8.318360284820657e-6
allele num: 120216
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.33G>A
  hgvsp: ENST00000313028.7:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.33G>A
  hgvsp: ENST00000532311.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.33G>A
  hgvsp: ENST00000529311.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+155G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.33G>A
  hgvsp: ENST00000528625.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.33G>A
  hgvsp: ENST00000529842.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.33G>A
  hgvsp: ENST00000528136.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.33G>A
  hgvsp: ENST00000525486.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.33G>A
  hgvsp: ENST00000528914.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.33G>A
  hgvsp: ENST00000313059.5:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.33G>A
  hgvsp: ENST00000527262.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.33G>A
  hgvsp: ENST00000531707.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.33G>A
  hgvsp: ENST00000530478.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.33G>A
  hgvsp: ENST00000525879.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.69G>A
  hgvsp: ENST00000525773.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.33G>A
  hgvsp: ENST00000531537.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.33G>A
  hgvsp: ENST00000524918.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.134G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val11Val
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-145060372-A-ACCCCTGCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060372
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060381
    reference: chr 8
allele count: 1
allele frequency: 8.738661586591398e-6
allele num: 114434
alternate allele: ACCCCTGCCC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.67_68insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.132_133insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.31_32insGGGCAGGGG
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly10_Val11insGlyAlaGly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-145060372-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060372
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060372
    reference: chr 8
allele count: 194
allele frequency: 1.695300347798731e-3
allele num: 114434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.32T>G
  hgvsp: ENSP00000434411.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.32T>G
  hgvsp: ENSP00000435161.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.68T>G
  hgvsp: ENSP00000434776.1:p.Val23Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.32T>G
  hgvsp: ENSP00000431818.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.32T>G
  hgvsp: ENSP00000325618.7:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.32T>G
  hgvsp: ENSP00000436697.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.32T>G
  hgvsp: ENSP00000431620.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.32T>G
  hgvsp: ENSP00000434005.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.32T>G
  hgvsp: ENSP00000432204.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.32T>G
  hgvsp: ENSP00000433990.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.133T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.32T>G
  hgvsp: ENSP00000436301.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.32T>G
  hgvsp: ENSP00000432733.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+154T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.32T>G
  hgvsp: ENSP00000435793.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.32T>G
  hgvsp: ENSP00000314320.5:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.32T>G
  hgvsp: ENSP00000431250.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.32T>G
  hgvsp: ENSP00000436333.1:p.Val11Gly
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val11Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

8-145060374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060374
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060374
    reference: chr 8
allele count: 2
allele frequency: 1.659310390601666e-5
allele num: 120532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.30G>A
  hgvsp: ENST00000524918.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.30G>A
  hgvsp: ENST00000525879.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.30G>A
  hgvsp: ENST00000529842.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.30G>A
  hgvsp: ENST00000528136.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.30G>A
  hgvsp: ENST00000313028.7:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.30G>A
  hgvsp: ENST00000525486.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.30G>A
  hgvsp: ENST00000528914.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.66G>A
  hgvsp: ENST00000525773.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.30G>A
  hgvsp: ENST00000531537.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.30G>A
  hgvsp: ENST00000530478.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.30G>A
  hgvsp: ENST00000313059.5:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.30G>A
  hgvsp: ENST00000527262.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.30G>A
  hgvsp: ENST00000532311.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+152G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.131G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.30G>A
  hgvsp: ENST00000528625.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.30G>A
  hgvsp: ENST00000531707.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.30G>A
  hgvsp: ENST00000529311.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly10Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

8-145060375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060375
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060375
    reference: chr 8
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.29G>A
  hgvsp: ENSP00000436301.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.29G>A
  hgvsp: ENSP00000435161.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.65G>A
  hgvsp: ENSP00000434776.1:p.Gly22Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.29G>A
  hgvsp: ENSP00000431818.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.29G>A
  hgvsp: ENSP00000434411.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.29G>A
  hgvsp: ENSP00000435793.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.29G>A
  hgvsp: ENSP00000432204.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+151G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.29G>A
  hgvsp: ENSP00000431620.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.29G>A
  hgvsp: ENSP00000436333.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.29G>A
  hgvsp: ENSP00000432733.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.29G>A
  hgvsp: ENSP00000431250.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.29G>A
  hgvsp: ENSP00000325618.7:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.29G>A
  hgvsp: ENSP00000434005.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.29G>A
  hgvsp: ENSP00000436697.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.29G>A
  hgvsp: ENSP00000433990.1:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.130G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.29G>A
  hgvsp: ENSP00000314320.5:p.Gly10Glu
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly10Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

8-145060378-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060378
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060378
    reference: chr 8
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.26C>G
  hgvsp: ENSP00000435793.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.26C>G
  hgvsp: ENSP00000435161.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.26C>G
  hgvsp: ENSP00000431818.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.26C>G
  hgvsp: ENSP00000325618.7:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.26C>G
  hgvsp: ENSP00000436301.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.26C>G
  hgvsp: ENSP00000434411.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.26C>G
  hgvsp: ENSP00000436333.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.26C>G
  hgvsp: ENSP00000314320.5:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.26C>G
  hgvsp: ENSP00000431620.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.26C>G
  hgvsp: ENSP00000434005.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.26C>G
  hgvsp: ENSP00000432733.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.62C>G
  hgvsp: ENSP00000434776.1:p.Ala21Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.127C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.26C>G
  hgvsp: ENSP00000432204.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.26C>G
  hgvsp: ENSP00000433990.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.26C>G
  hgvsp: ENSP00000431250.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.26C>G
  hgvsp: ENSP00000436697.1:p.Ala9Gly
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+148C>G
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala9Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

8-145060383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060383
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060383
    reference: chr 8
allele count: 1
allele frequency: 8.29324929507381e-6
allele num: 120580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.21A>G
  hgvsp: ENST00000530478.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.21A>G
  hgvsp: ENST00000532311.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.21A>G
  hgvsp: ENST00000531707.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.21A>G
  hgvsp: ENST00000531537.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.21A>G
  hgvsp: ENST00000528136.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.21A>G
  hgvsp: ENST00000525879.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.21A>G
  hgvsp: ENST00000313028.7:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.21A>G
  hgvsp: ENST00000313059.5:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.21A>G
  hgvsp: ENST00000528914.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.21A>G
  hgvsp: ENST00000529311.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.57A>G
  hgvsp: ENST00000525773.1:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.21A>G
  hgvsp: ENST00000527262.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.21A>G
  hgvsp: ENST00000528625.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.21A>G
  hgvsp: ENST00000529842.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.21A>G
  hgvsp: ENST00000524918.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.21A>G
  hgvsp: ENST00000525486.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+143A>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.122A>G
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala7Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

8-145060383-T-TGCCTCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060383
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060389
    reference: chr 8
allele count: 3
allele frequency: 2.487974788522143e-5
allele num: 120580
alternate allele: TGCCTCC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000431818.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000436301.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000431620.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000432204.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000434005.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000436697.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.15_20dupGGAGGC
  hgvsp: ENSP00000325618.7:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000433990.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.51_56dupGGAGGC
  hgvsp: ENSP00000434776.1:p.Glu18_Ala19dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.116_121dupGGAGGC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000435161.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000436333.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+137_97+142dupGGAGGC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000432733.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000435793.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000431250.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.15_20dupGGAGGC
  hgvsp: ENSP00000314320.5:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.15_20dupGGAGGC
  hgvsp: ENSP00000434411.1:p.Glu6_Ala7dup
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu6_Ala7dup
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

8-145060386-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060386
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060386
    reference: chr 8
allele count: 2
allele frequency: 1.658292290599141e-5
allele num: 120606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.18G>C
  hgvsp: ENSP00000434005.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.18G>C
  hgvsp: ENSP00000436301.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.18G>C
  hgvsp: ENSP00000436697.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.18G>C
  hgvsp: ENSP00000432204.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.18G>C
  hgvsp: ENSP00000433990.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.18G>C
  hgvsp: ENSP00000435793.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+140G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.18G>C
  hgvsp: ENSP00000314320.5:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.18G>C
  hgvsp: ENSP00000436333.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.18G>C
  hgvsp: ENSP00000325618.7:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.18G>C
  hgvsp: ENSP00000431620.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.18G>C
  hgvsp: ENSP00000434411.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.18G>C
  hgvsp: ENSP00000432733.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.119G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.18G>C
  hgvsp: ENSP00000431818.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.18G>C
  hgvsp: ENSP00000431250.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.54G>C
  hgvsp: ENSP00000434776.1:p.Glu18Asp
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.18G>C
  hgvsp: ENSP00000435161.1:p.Glu6Asp
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu6Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

8-145060389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060389
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060389
    reference: chr 8
allele count: 3
allele frequency: 2.487273450843186e-5
allele num: 120614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.15G>A
  hgvsp: ENST00000524918.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+137G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.15G>A
  hgvsp: ENST00000527262.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.51G>A
  hgvsp: ENST00000525773.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.15G>A
  hgvsp: ENST00000529311.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.15G>A
  hgvsp: ENST00000525879.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.15G>A
  hgvsp: ENST00000529842.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.15G>A
  hgvsp: ENST00000525486.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.15G>A
  hgvsp: ENST00000528914.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.15G>A
  hgvsp: ENST00000530478.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.116G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.15G>A
  hgvsp: ENST00000528625.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.15G>A
  hgvsp: ENST00000313028.7:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.15G>A
  hgvsp: ENST00000532311.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.15G>A
  hgvsp: ENST00000531707.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.15G>A
  hgvsp: ENST00000531537.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.15G>A
  hgvsp: ENST00000313059.5:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.15G>A
  hgvsp: ENST00000528136.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala5Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

8-145060390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060390
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060390
    reference: chr 8
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.14C>T
  hgvsp: ENSP00000432733.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.14C>T
  hgvsp: ENSP00000435793.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.14C>T
  hgvsp: ENSP00000431250.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.14C>T
  hgvsp: ENSP00000436697.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.50C>T
  hgvsp: ENSP00000434776.1:p.Ala17Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.14C>T
  hgvsp: ENSP00000325618.7:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.14C>T
  hgvsp: ENSP00000431620.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.14C>T
  hgvsp: ENSP00000436301.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.14C>T
  hgvsp: ENSP00000432204.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.14C>T
  hgvsp: ENSP00000436333.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.14C>T
  hgvsp: ENSP00000433990.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.14C>T
  hgvsp: ENSP00000435161.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.14C>T
  hgvsp: ENSP00000434411.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+136C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.115C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.14C>T
  hgvsp: ENSP00000314320.5:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.14C>T
  hgvsp: ENSP00000431818.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.14C>T
  hgvsp: ENSP00000434005.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala5Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/8-145060399-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060399
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060400
    reference: chr 8
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.4dupG
  hgvsp: ENSP00000433990.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+126dupG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.40dupG
  hgvsp: ENSP00000434776.1:p.Val14GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.4dupG
  hgvsp: ENSP00000434411.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.4dupG
  hgvsp: ENSP00000435793.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.4dupG
  hgvsp: ENSP00000436333.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.4dupG
  hgvsp: ENSP00000434005.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.4dupG
  hgvsp: ENSP00000435161.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.4dupG
  hgvsp: ENSP00000432204.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.4dupG
  hgvsp: ENSP00000436301.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.4dupG
  hgvsp: ENSP00000431818.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.4dupG
  hgvsp: ENSP00000436697.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.105dupG
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.4dupG
  hgvsp: ENSP00000431620.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.4dupG
  hgvsp: ENSP00000314320.5:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.4dupG
  hgvsp: ENSP00000325618.7:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.4dupG
  hgvsp: ENSP00000431250.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.4dupG
  hgvsp: ENSP00000432733.1:p.Val2GlyfsTer31
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val2GlyfsTer31
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-145060399-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060399
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060399
    reference: chr 8
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.5T>C
  hgvsp: ENSP00000436301.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.5T>C
  hgvsp: ENSP00000431250.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.5T>C
  hgvsp: ENSP00000433990.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.106T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.41T>C
  hgvsp: ENSP00000434776.1:p.Val14Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.5T>C
  hgvsp: ENSP00000436333.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.5T>C
  hgvsp: ENSP00000314320.5:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.5T>C
  hgvsp: ENSP00000431818.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+127T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.5T>C
  hgvsp: ENSP00000435161.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.5T>C
  hgvsp: ENSP00000434411.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.5T>C
  hgvsp: ENSP00000431620.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.5T>C
  hgvsp: ENSP00000435793.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.5T>C
  hgvsp: ENSP00000434005.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.5T>C
  hgvsp: ENSP00000432733.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.5T>C
  hgvsp: ENSP00000436697.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.5T>C
  hgvsp: ENSP00000432204.1:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.5T>C
  hgvsp: ENSP00000325618.7:p.Val2Ala
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val2Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

8-145060400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060400
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060400
    reference: chr 8
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.4G>A
  hgvsp: ENSP00000435161.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.4G>A
  hgvsp: ENSP00000435793.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.4G>A
  hgvsp: ENSP00000436333.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.4G>A
  hgvsp: ENSP00000431250.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.4G>A
  hgvsp: ENSP00000434411.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.4G>A
  hgvsp: ENSP00000314320.5:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.105G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.4G>A
  hgvsp: ENSP00000436697.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.4G>A
  hgvsp: ENSP00000432733.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+126G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.4G>A
  hgvsp: ENSP00000431620.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.4G>A
  hgvsp: ENSP00000432204.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.4G>A
  hgvsp: ENSP00000436301.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.4G>A
  hgvsp: ENSP00000325618.7:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.4G>A
  hgvsp: ENSP00000431818.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.40G>A
  hgvsp: ENSP00000434776.1:p.Val14Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.4G>A
  hgvsp: ENSP00000433990.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.4G>A
  hgvsp: ENSP00000434005.1:p.Val2Ile
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val2Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-145060404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060404
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060404
    reference: chr 8
allele count: 3
allele frequency: 2.485254158658626e-5
allele num: 120712
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.36C>T
  hgvsp: ENST00000525773.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+122C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-3C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3-3C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

8-145060407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060407
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060407
    reference: chr 8
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.33T>C
  hgvsp: ENST00000525773.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+119T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-6T>C
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3-6T>C
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/8-145060408-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060408
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060408
    reference: chr 8
allele count: 12
allele frequency: 9.938546653194415e-5
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.32G>T
  hgvsp: ENSP00000434776.1:p.Arg11Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+118G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-7G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-145060408-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060408
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060408
    reference: chr 8
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+118G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.32G>A
  hgvsp: ENSP00000434776.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-7G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11His
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-145060409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060409
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060409
    reference: chr 8
allele count: 2
allele frequency: 1.655656550605143e-5
allele num: 120798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.31C>T
  hgvsp: ENSP00000434776.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+117C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-8C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17432
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11Cys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

8-145060411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060411
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060411
    reference: chr 8
allele count: 3
allele frequency: 2.482786016949153e-5
allele num: 120832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.29C>T
  hgvsp: ENSP00000434776.1:p.Pro10Leu
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+115C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-10C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro10Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-145060416-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060416
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060416
    reference: chr 8
allele count: 2
allele frequency: 1.654533421575116e-5
allele num: 120880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.24G>C
  hgvsp: ENST00000525773.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+110G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-15G>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-15G>C
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu8Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

8-145060422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060422
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060422
    reference: chr 8
allele count: 6
allele frequency: 4.958923582987586e-5
allele num: 120994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.18C>T
  hgvsp: ENST00000525773.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-21C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+104C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr6Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-145060427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060427
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060427
    reference: chr 8
allele count: 5
allele frequency: 4.130934086815711e-5
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.13C>T
  hgvsp: ENSP00000434776.1:p.Pro5Ser
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+99C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-26C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro5Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

8-145060436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060436
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060436
    reference: chr 8
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+90G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.4G>A
  hgvsp: ENSP00000434776.1:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-35G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly2Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-145060440-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060440
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060440
    reference: chr 8
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-1A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+86A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-39A>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

8-145060441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060441
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060441
    reference: chr 8
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-2G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+85G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-40G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-145060444-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060444
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060444
    reference: chr 8
allele count: 3
allele frequency: 2.4786014078456e-5
allele num: 121036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-5G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+82G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-43G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

8-145060451-TGCCCCTCCCCAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060451
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060439
    reference: chr 8
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: TGCCCCTCCCCAG
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-145060458-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060458
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060458
    reference: chr 8
allele count: 32
allele frequency: 2.642444260941371e-4
allele num: 121100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+68G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-19G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-57G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-145060460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060460
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060460
    reference: chr 8
allele count: 3
allele frequency: 2.477414240177052e-5
allele num: 121094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+66G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.104-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-21G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.3-59G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

8-145060464-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060464
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060464
    reference: chr 8
allele count: 3
allele frequency: 2.476800634060962e-5
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-25C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+62C>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

8-145060465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060465
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060465
    reference: chr 8
allele count: 5
allele frequency: 4.127932896322837e-5
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-26G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+61G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17751
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-145060471-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060471
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060471
    reference: chr 8
allele count: 9
allele frequency: 7.429665830141328e-5
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-32G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+55G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/8-145060473-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060473
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060473
    reference: chr 8
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-34T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+53T>G
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17791
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

8-145060479-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060479
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060479
    reference: chr 8
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-40C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+47C>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-145060488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060488
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060488
    reference: chr 8
allele count: 3
allele frequency: 2.47537006782514e-5
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+38C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

8-145060491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060491
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060491
    reference: chr 8
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-52G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+35G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-145060502-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060502
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060502
    reference: chr 8
allele count: 27
allele frequency: 2.22680412371134e-4
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-63C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+24C>G
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-145060504-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060504
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060503
    reference: chr 8
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-66delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+21delC
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: TG
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

8-145060506-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060506
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060506
    reference: chr 8
allele count: 3
allele frequency: 2.474104374216534e-5
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-67C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+20C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+20C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/8-145060516-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060516
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060516
    reference: chr 8
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-77G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+10G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-145060516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060516
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060516
    reference: chr 8
allele count: 2
allele frequency: 1.649158104787506e-5
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-77G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+10G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-145060517-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060517
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060517
    reference: chr 8
allele count: 11
allele frequency: 9.070219994063128e-5
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-78T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+9T>C
  variant of: http://identifiers.org/hgnc/25895
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

8-145060525-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060525
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060525
    reference: chr 8
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.103+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.550G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-86G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.2+1G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.97+1G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2+1G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-145060532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060532
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060532
    reference: chr 8
allele count: 11
allele frequency: 9.070967954744116e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.544G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.543G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.91G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-93G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.97G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-5G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

8-145060533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060533
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060533
    reference: chr 8
allele count: 3
allele frequency: 2.47390035129385e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.542C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.96C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.543C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-94C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.90C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-6C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

8-145060538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060538
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060538
    reference: chr 8
allele count: 6
allele frequency: 4.9478007025877e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.537G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.538G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-99G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.85G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.91G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-11G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

8-145060539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060539
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060539
    reference: chr 8
allele count: 3
allele frequency: 2.473981956424931e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.536C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.537C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.84C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-100C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.90C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-145060539-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060539
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060539
    reference: chr 8
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.537C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.536C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.84C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.90C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-100C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-12C>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-145060544-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060544
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060544
    reference: chr 8
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-105C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.531C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.85C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.532C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.79C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-17C>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/8-145060549-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060549
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060549
    reference: chr 8
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-110G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.526G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.527G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.80G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.74G>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

8-145060559-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060559
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060559
    reference: chr 8
allele count: 36
allele frequency: 2.969121140142518e-4
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.516C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-120C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.64C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.517C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.70C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

8-145060562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060562
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060562
    reference: chr 8
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.514G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.61G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-123G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.513G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.67G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-35G>A
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

8-145060571-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060571
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060571
    reference: chr 8
allele count: 13
allele frequency: 1.072129579230376e-4
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.504C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.58C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.52C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-132C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.505C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-44C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17672
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

8-145060578-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 145060578
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 145060578
    reference: chr 8
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000314320
  ensembl transcript: ENST00000313059
  gene symbol: PARP10
  hgvsc: ENST00000313059.5:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436333
  ensembl transcript: ENST00000530478
  gene symbol: PARP10
  hgvsc: ENST00000530478.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000433990
  ensembl transcript: ENST00000531707
  gene symbol: PARP10
  hgvsc: ENST00000531707.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000325618
  ensembl transcript: ENST00000313028
  gene symbol: PARP10
  hgvsc: ENST00000313028.7:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434776
  ensembl transcript: ENST00000525773
  gene symbol: PARP10
  hgvsc: ENST00000525773.1:c.-139C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436697
  ensembl transcript: ENST00000529842
  gene symbol: PARP10
  hgvsc: ENST00000529842.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434005
  ensembl transcript: ENST00000528914
  gene symbol: PARP10
  hgvsc: ENST00000528914.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431620
  ensembl transcript: ENST00000524918
  gene symbol: PARP10
  hgvsc: ENST00000524918.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000436301
  ensembl transcript: ENST00000525879
  gene symbol: PARP10
  hgvsc: ENST00000525879.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000528580
  gene symbol: PARP10
  hgvsc: ENST00000528580.1:n.51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000533665
  gene symbol: PARP10
  hgvsc: ENST00000533665.1:n.45C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000534737
  gene symbol: PARP10
  hgvsc: ENST00000534737.1:n.497C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435793
  ensembl transcript: ENST00000525486
  gene symbol: PARP10
  hgvsc: ENST00000525486.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000434411
  ensembl transcript: ENST00000529311
  gene symbol: PARP10
  hgvsc: ENST00000529311.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432204
  ensembl transcript: ENST00000531537
  gene symbol: PARP10
  hgvsc: ENST00000531537.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000432733
  ensembl transcript: ENST00000527262
  gene symbol: PARP10
  hgvsc: ENST00000527262.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431250
  ensembl transcript: ENST00000528136
  gene symbol: PARP10
  hgvsc: ENST00000528136.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000431818
  ensembl transcript: ENST00000528625
  gene symbol: PARP10
  hgvsc: ENST00000528625.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178685
  ensembl transcript: ENST00000532660
  gene symbol: PARP10
  hgvsc: ENST00000532660.1:n.498C>T
  variant of: http://identifiers.org/hgnc/25895
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000178685
  ensembl protein: ENSP00000435161
  ensembl transcript: ENST00000532311
  gene symbol: PARP10
  hgvsc: ENST00000532311.1:c.-51C>T
  variant of: http://identifiers.org/hgnc/25895
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 88
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29373
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7521
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 888
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17756
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 751
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1901
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 24
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36015
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 1.097e0

QD
type: SiteQuality
SIO_000300: 1.129e1

DP
type: SiteQuality
SIO_000300: 1.559792e6

GenotypeDepth
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 751
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1901
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17756
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29373
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 888
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36015
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517680983457277e-5
allele num: 65890
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.129e1

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

DP
type: SiteQuality
SIO_000300: 1.559792e6

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.35e-1

FS
type: SiteQuality
SIO_000300: 1.097e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-2

GenotypeDepth
all individuals: 29318
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1915
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17751
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 770
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 383
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7520
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 292
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65888
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.597402597402597e-4
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.22e0

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.87e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 1.560769e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e0

QD
type: SiteQuality
SIO_000300: 1.188e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.249e0

VQSLOD
type: SiteQuality
SIO_000300: -2.096e-1

GenotypeDepth
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 758
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29333
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7514
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 877
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1902
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17780
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 71
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36173
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517266492686776e-5
allele num: 65908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 8.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e0

MQ
type: SiteQuality
SIO_000300: 5.794e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.962e0

MQRankSum
type: SiteQuality
SIO_000300: 3.25e0

FS
type: SiteQuality
SIO_000300: 5.59e0

VQSLOD
type: SiteQuality
SIO_000300: -3.779e0

DP
type: SiteQuality
SIO_000300: 1.559927e6

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29272
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7417
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 995
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17731
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1845
bin: 3.75e1
variant carriers: 0

GenotypeDepth
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FS
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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Latino
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East Asian
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African
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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Latino
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East Asian
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European (Finnish)
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South Asian
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MQ
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ReadPosRankSum
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South Asian
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Latino
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GenotypeQuality
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bin: 6.25e1
variant carriers: 5

GenotypeQuality
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bin: 2.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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bin: 3.25e1
variant carriers: 5

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 6

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 1869
bin: 9.75e1
variant carriers: 122

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 113
allele frequency: 1.808694538702862e-3
allele num: 62476
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.222493887530562e-3
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.89066918001885e-4
allele num: 8488
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.287001287001287e-3
allele num: 9324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 51
allele frequency: 9.333821376281113e-3
allele num: 5464
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.506926179203928e-4
allele num: 11406
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.860857941426662e-4
allele num: 16458
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.466e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.952e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

QD
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

DP
type: SiteQuality
SIO_000300: 1.639334e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e0

FS
type: SiteQuality
SIO_000300: 1.33601e2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.106e1

GenotypeDepth
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17169
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variant carriers: 0

GenotypeDepth
all individuals: 571
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variant carriers: 0

GenotypeDepth
all individuals: 270
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variant carriers: 0

GenotypeDepth
all individuals: 219
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variant carriers: 0

GenotypeDepth
all individuals: 348
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variant carriers: 0

GenotypeDepth
all individuals: 967
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2069
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 395
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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
all individuals: 735
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2372
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variant carriers: 0

GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 265
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 759
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variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 34512
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 964
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.223e1

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.832e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-1

DP
type: SiteQuality
SIO_000300: 1.708068e6

MQ
type: SiteQuality
SIO_000300: 5.918e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

GenotypeDepth
all individuals: 967
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17156
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variant carriers: 0

GenotypeDepth
all individuals: 400
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variant carriers: 0

GenotypeDepth
all individuals: 677
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variant carriers: 0

GenotypeDepth
all individuals: 458
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variant carriers: 0

GenotypeDepth
all individuals: 31
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variant carriers: 0

GenotypeDepth
all individuals: 734
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variant carriers: 1

GenotypeDepth
all individuals: 28072
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variant carriers: 0

GenotypeDepth
all individuals: 571
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variant carriers: 0

GenotypeDepth
all individuals: 270
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variant carriers: 0

GenotypeDepth
all individuals: 395
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variant carriers: 0

GenotypeDepth
all individuals: 180
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variant carriers: 0

GenotypeDepth
all individuals: 161
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variant carriers: 0

GenotypeDepth
all individuals: 7364
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GenotypeDepth
all individuals: 231
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variant carriers: 0

GenotypeDepth
all individuals: 219
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variant carriers: 0

GenotypeDepth
all individuals: 225
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variant carriers: 0

GenotypeDepth
all individuals: 350
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variant carriers: 0

GenotypeDepth
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 964
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 741
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2372
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variant carriers: 0

GenotypeQuality
all individuals: 8442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34434
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variant carriers: 0

GenotypeQuality
all individuals: 3440
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variant carriers: 0

GenotypeQuality
all individuals: 4450
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variant carriers: 1

GenotypeQuality
all individuals: 3775
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66150
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.932e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 5.135e1

QD
type: SiteQuality
SIO_000300: 8.27e0

FS
type: SiteQuality
SIO_000300: 2.422e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.708296e6

GenotypeDepth
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17167
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variant carriers: 0

GenotypeDepth
all individuals: 966
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variant carriers: 0

GenotypeDepth
all individuals: 172
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variant carriers: 0

GenotypeDepth
all individuals: 654
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variant carriers: 0

GenotypeDepth
all individuals: 225
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variant carriers: 0

GenotypeDepth
all individuals: 735
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 219
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GenotypeDepth
all individuals: 401
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variant carriers: 0

GenotypeDepth
all individuals: 7362
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variant carriers: 0

GenotypeDepth
all individuals: 391
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GenotypeDepth
all individuals: 28146
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variant carriers: 0

GenotypeDepth
all individuals: 2069
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variant carriers: 0

GenotypeDepth
all individuals: 349
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GenotypeDepth
all individuals: 570
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GenotypeDepth
all individuals: 180
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variant carriers: 0

GenotypeDepth
all individuals: 270
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GenotypeDepth
all individuals: 161
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 4452
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variant carriers: 1

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3442
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 8456
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variant carriers: 0

GenotypeQuality
all individuals: 2369
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variant carriers: 0

GenotypeQuality
all individuals: 244
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
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variant carriers: 0

GenotypeQuality
all individuals: 962
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variant carriers: 0

GenotypeQuality
all individuals: 34594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.532e1

DP
type: SiteQuality
SIO_000300: 1.709003e6

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
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SIO_000300: -7.21e-1

FS
type: SiteQuality
SIO_000300: 2.282e0

ReadPosRankSum
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SIO_000300: 1.47e0

ClippingRankSum
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SIO_000300: -1.0e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 8.44e-1

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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bin: 4.75e1
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 25
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GenotypeDepth
all individuals: 172
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GenotypeDepth
all individuals: 966
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GenotypeDepth
all individuals: 219
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GenotypeDepth
all individuals: 401
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GenotypeDepth
all individuals: 376
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GenotypeDepth
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 70
bin: 4.75e1
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GenotypeQuality
all individuals: 979
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 34673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 697
bin: 2.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511076188461422e-5
allele num: 66178
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.97e0

MQ
type: SiteQuality
SIO_000300: 5.041e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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SIO_000300: 1.07e0

BaseQRankSum
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SIO_000300: -1.05e0

ClippingRankSum
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SIO_000300: -7.35e-1

DP
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SIO_000300: 1.710376e6

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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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 34673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

African
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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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European (Non-Finnish)
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 (Finnish)
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Other
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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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FS
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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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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Latino
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allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

African
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East Asian
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66272
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

DP
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SIO_000300: 1.714429e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.087e1

MQRankSum
type: SiteQuality
SIO_000300: 7.98e-1

MQ
type: SiteQuality
SIO_000300: 6.082e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

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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GenotypeDepth
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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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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

GenotypeQuality
all individuals: 17
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508705229172324e-5
allele num: 66282
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -6.074e0

MQRankSum
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SIO_000300: 1.11e0

VQSLOD
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SIO_000300: 1.23e0

QD
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SIO_000300: 1.471e1

FS
type: SiteQuality
SIO_000300: 3.044e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ReadPosRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.714574e6

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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variant carriers: 0

GenotypeDepth
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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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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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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8534
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variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016864271276435e-5
allele num: 66294
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

DP
type: SiteQuality
SIO_000300: 1.715261e6

QD
type: SiteQuality
SIO_000300: 1.521e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.488e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

FS
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeDepth
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bin: 7.25e1
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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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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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4470
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

DP
type: SiteQuality
SIO_000300: 1.715705e6

FS
type: SiteQuality
SIO_000300: 1.143e0

InbreedingCoeff
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SIO_000300: -4.0e-4

ReadPosRankSum
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SIO_000300: 1.32e0

BaseQRankSum
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SIO_000300: 6.23e0

ClippingRankSum
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SIO_000300: -5.86e-1

VQSLOD
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SIO_000300: 3.83e-1

QD
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SIO_000300: 1.455e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

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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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 51
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.778994719342852e-5
allele num: 10226
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 11
allele frequency: 1.658574831880824e-4
allele num: 66322
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
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MQRankSum
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SIO_000300: 6.44e-1

VQSLOD
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 156
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 2388
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4482
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3465
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variant carriers: 0

GenotypeQuality
all individuals: 985
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variant carriers: 0

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

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

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

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 26
allele frequency: 3.906367378827489e-4
allele num: 66558
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 4.320774282751469e-4
allele num: 11572
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

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

MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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QD
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SIO_000300: 1.317e1

MQ
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SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 1.733096e6

InbreedingCoeff
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SIO_000300: -4.0e-4

ClippingRankSum
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SIO_000300: -4.13e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

South Asian
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allele frequency: 1.827262760384943e-4
allele num: 16418
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Other
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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
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -8.71e-1

MQ
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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SIO_000300: 9.389999999999999e-1

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.506399086703119e-5
allele num: 66572
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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SIO_000300: 5.961e1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: -1.21e-1

ClippingRankSum
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SIO_000300: 8.53e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

DP
type: SiteQuality
SIO_000300: 1.733596e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

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: 4
allele frequency: 3.849855630413859e-4
allele num: 10390
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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South Asian
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allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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Latino
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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SIO_000300: 5.978e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 9
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allele num: 66588
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Latino
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num of homozygotes: 0

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