15-72556916-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556916
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556916
    reference: chr 15
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.375G>C
  hgvsp: ENST00000419739.3:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.375G>C
  hgvsp: ENST00000569795.1:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.233G>C
  hgvsp: ENST00000567974.1:c.233G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*245G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1199G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.375G>C
  hgvsp: ENST00000565443.1:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.578G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.375G>C
  hgvsp: ENST00000260376.7:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.375G>C
  hgvsp: ENST00000567440.1:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.375G>C
  hgvsp: ENST00000287196.9:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.232G>C
  hgvsp: ENST00000564610.1:c.232G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly125Gly
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-72556921-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556921
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556921
    reference: chr 15
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1194T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.573T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.370T>C
  hgvsp: ENSP00000454298.1:p.Phe124Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.227T>C
  hgvsp: ENSP00000456468.1:p.Phe77Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.370T>C
  hgvsp: ENSP00000287196.9:p.Phe124Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*240T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.228T>C
  hgvsp: ENSP00000455815.1:p.Phe77Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.370T>C
  hgvsp: ENSP00000260376.7:p.Phe124Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.370T>C
  hgvsp: ENSP00000456348.1:p.Phe124Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.370T>C
  hgvsp: ENSP00000403265.3:p.Phe124Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.370T>C
  hgvsp: ENSP00000456370.1:p.Phe124Leu
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe124Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

15-72556925-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556925
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556925
    reference: chr 15
allele count: 3
allele frequency: 2.484677820109326e-5
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.366A>G
  hgvsp: ENST00000260376.7:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.569A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.366A>G
  hgvsp: ENST00000565443.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.366A>G
  hgvsp: ENST00000567440.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.224A>G
  hgvsp: ENST00000567974.1:c.224A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.223A>G
  hgvsp: ENST00000564610.1:c.223A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.366A>G
  hgvsp: ENST00000419739.3:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1190A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.366A>G
  hgvsp: ENST00000569795.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*236A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.366A>G
  hgvsp: ENST00000287196.9:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu122Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

15-72556932-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556932
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556932
    reference: chr 15
allele count: 2
allele frequency: 1.656479318855704e-5
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.359A>G
  hgvsp: ENSP00000260376.7:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.216A>G
  hgvsp: ENSP00000456468.1:p.Asn73Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.359A>G
  hgvsp: ENSP00000403265.3:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.359A>G
  hgvsp: ENSP00000454298.1:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.359A>G
  hgvsp: ENSP00000456348.1:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.359A>G
  hgvsp: ENSP00000456370.1:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.217A>G
  hgvsp: ENSP00000455815.1:p.Asn73Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*229A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.562A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.359A>G
  hgvsp: ENSP00000287196.9:p.Asn120Ser
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1183A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn120Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

15-72556933-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556933
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556933
    reference: chr 15
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.358A>G
  hgvsp: ENSP00000456348.1:p.Asn120Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.358A>G
  hgvsp: ENSP00000403265.3:p.Asn120Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.358A>G
  hgvsp: ENSP00000454298.1:p.Asn120Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1182A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.358A>G
  hgvsp: ENSP00000456370.1:p.Asn120Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.216A>G
  hgvsp: ENSP00000455815.1:p.Asn73Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.561A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.358A>G
  hgvsp: ENSP00000260376.7:p.Asn120Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*228A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.358A>G
  hgvsp: ENSP00000287196.9:p.Asn120Asp
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.215A>G
  hgvsp: ENSP00000456468.1:p.Asn73Asp
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn120Asp
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

15-72556938-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556938
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556938
    reference: chr 15
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.353C>T
  hgvsp: ENSP00000456348.1:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.353C>T
  hgvsp: ENSP00000454298.1:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.353C>T
  hgvsp: ENSP00000260376.7:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.211C>T
  hgvsp: ENSP00000455815.1:p.Pro71Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.353C>T
  hgvsp: ENSP00000456370.1:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.353C>T
  hgvsp: ENSP00000403265.3:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.353C>T
  hgvsp: ENSP00000287196.9:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.210C>T
  hgvsp: ENSP00000456468.1:p.Pro71Leu
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.556C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*223C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1177C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro118Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

15-72556948-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556948
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556948
    reference: chr 15
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.546G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.343G>A
  hgvsp: ENSP00000260376.7:p.Val115Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.200G>A
  hgvsp: ENSP00000456468.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*213G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.343G>A
  hgvsp: ENSP00000403265.3:p.Val115Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.343G>A
  hgvsp: ENSP00000456348.1:p.Val115Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.343G>A
  hgvsp: ENSP00000454298.1:p.Val115Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.201G>A
  hgvsp: ENSP00000455815.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.343G>A
  hgvsp: ENSP00000287196.9:p.Val115Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.343G>A
  hgvsp: ENSP00000456370.1:p.Val115Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1167G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12438
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val115Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

15-72556954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556954
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556954
    reference: chr 15
allele count: 2
allele frequency: 1.656698861847882e-5
allele num: 120722
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.337A>G
  hgvsp: ENSP00000456348.1:p.Ile113Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.337A>G
  hgvsp: ENSP00000287196.9:p.Ile113Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.337A>G
  hgvsp: ENSP00000260376.7:p.Ile113Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*207A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.540A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.337A>G
  hgvsp: ENSP00000456370.1:p.Ile113Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1161A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.337A>G
  hgvsp: ENSP00000454298.1:p.Ile113Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.195A>G
  hgvsp: ENSP00000455815.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.194A>G
  hgvsp: ENSP00000456468.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.337A>G
  hgvsp: ENSP00000403265.3:p.Ile113Val
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile113Val
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

15-72556958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556958
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556958
    reference: chr 15
allele count: 2
allele frequency: 1.656808655168415e-5
allele num: 120714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*203A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.333A>G
  hgvsp: ENST00000419739.3:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.333A>G
  hgvsp: ENST00000287196.9:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1157A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.333A>G
  hgvsp: ENST00000260376.7:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.190A>G
  hgvsp: ENST00000564610.1:c.190A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.536A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.333A>G
  hgvsp: ENST00000569795.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.333A>G
  hgvsp: ENST00000565443.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.191A>G
  hgvsp: ENST00000567974.1:c.191A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.333A>G
  hgvsp: ENST00000567440.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro111Pro
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

15-72556965-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556965
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556965
    reference: chr 15
allele count: 4
allele frequency: 3.314111486710413e-5
allele num: 120696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-3C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-3C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.329-3C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

15-72556977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556977
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556977
    reference: chr 15
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-15C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-15C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-72556986-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556986
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556986
    reference: chr 15
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-24A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

15-72556989-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556989
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556989
    reference: chr 15
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-27A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-27A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

15-72556995-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556995
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556995
    reference: chr 15
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-33G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-33G>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

15-72556995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556995
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556995
    reference: chr 15
allele count: 36
allele frequency: 2.986857825567503e-4
allele num: 120528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-33G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-33G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12018
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

15-72556996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556996
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556996
    reference: chr 15
allele count: 1
allele frequency: 8.295588406085643e-6
allele num: 120546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-34T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-34T>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

15-72556998-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72556998
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72556997
    reference: chr 15
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-37delA
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-37delA
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: AT
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

15-72557003-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557003
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557003
    reference: chr 15
allele count: 1
allele frequency: 8.29985724245543e-6
allele num: 120484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-41A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-41A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-72557009-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557009
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557008
    reference: chr 15
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-48delG
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-48delG
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: TC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-72557014-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557014
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557014
    reference: chr 15
allele count: 5
allele frequency: 4.158280800385889e-5
allele num: 120242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.329-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.329-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.329-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.186-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1153-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.329-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.329-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*199-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.329-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.532-52C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.187-52C>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9736
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9377
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

15-72557378-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557378
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557378
    reference: chr 15
allele count: 2
allele frequency: 1.803654203416121e-5
allele num: 110886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+44C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+44C>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-72557380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557380
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557380
    reference: chr 15
allele count: 1
allele frequency: 8.985694773919919e-6
allele num: 111288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+42G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+42G>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

15-72557381-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557381
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557381
    reference: chr 15
allele count: 2
allele frequency: 1.795396603109627e-5
allele num: 111396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+41G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+41G>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

15-72557385-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557385
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557385
    reference: chr 15
allele count: 10
allele frequency: 8.930804129603829e-5
allele num: 111972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+37G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+37G>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11894
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

15-72557392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557392
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557392
    reference: chr 15
allele count: 23
allele frequency: 2.039549525583045e-4
allele num: 112770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+30G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+30G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23391
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

15-72557394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557394
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557394
    reference: chr 15
allele count: 1
allele frequency: 8.834078340606724e-6
allele num: 113198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+28G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+28G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-72557398-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557398
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557398
    reference: chr 15
allele count: 1
allele frequency: 8.781327385447585e-6
allele num: 113878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+24G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+24G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD

15-72557401-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557401
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557401
    reference: chr 15
allele count: 13
allele frequency: 1.137238435159913e-4
allele num: 114312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+21C>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+21C>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27023
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14186
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-72557415-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557415
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557415
    reference: chr 15
allele count: 4
allele frequency: 3.438257491103509e-5
allele num: 116338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+7G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+7G>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30241
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.328+7G>C
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

15-72557416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557416
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557416
    reference: chr 15
allele count: 1
allele frequency: 8.585901948999742e-6
allele num: 116470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+6G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+6G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30348
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.328+6G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

15-72557418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557418
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557418
    reference: chr 15
allele count: 3
allele frequency: 2.572192880170108e-5
allele num: 116632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+4A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+4A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.328+4A>G
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

15-72557419-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557419
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557419
    reference: chr 15
allele count: 1
allele frequency: 8.565603960735272e-6
allele num: 116746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.186+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.328+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.328+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.328+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.328+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*198+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.328+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.328+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.185+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.531+3A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1152+3A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.328+3A>G
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: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

15-72557443-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557443
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557443
    reference: chr 15
allele count: 3
allele frequency: 2.543795682330795e-5
allele num: 117934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.165T>C
  hgvsp: ENSP00000455815.1:p.Ser56Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.307T>C
  hgvsp: ENSP00000454298.1:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.307T>C
  hgvsp: ENSP00000456348.1:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*177T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.164T>C
  hgvsp: ENSP00000456468.1:p.Ser56Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.307T>C
  hgvsp: ENSP00000456370.1:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.307T>C
  hgvsp: ENSP00000260376.7:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1131T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.307T>C
  hgvsp: ENSP00000287196.9:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.510T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.307T>C
  hgvsp: ENSP00000403265.3:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31092
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser103Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

15-72557464-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557464
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557464
    reference: chr 15
allele count: 1
allele frequency: 8.48032564450475e-6
allele num: 117920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.144T>C
  hgvsp: ENST00000567974.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*156T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1110T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.286T>C
  hgvsp: ENST00000260376.7:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.286T>C
  hgvsp: ENST00000569795.1:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.143T>C
  hgvsp: ENST00000564610.1:c.143T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.286T>C
  hgvsp: ENST00000565443.1:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.489T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.286T>C
  hgvsp: ENST00000287196.9:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.286T>C
  hgvsp: ENST00000419739.3:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.286T>C
  hgvsp: ENST00000567440.1:c.286T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu96Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-72557470-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557470
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557470
    reference: chr 15
allele count: 4
allele frequency: 3.400608708958904e-5
allele num: 117626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.138A>G
  hgvsp: ENSP00000455815.1:p.Ile47Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.280A>G
  hgvsp: ENSP00000287196.9:p.Ile94Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.280A>G
  hgvsp: ENSP00000454298.1:p.Ile94Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.280A>G
  hgvsp: ENSP00000456370.1:p.Ile94Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1104A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.483A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*150A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.280A>G
  hgvsp: ENSP00000456348.1:p.Ile94Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.280A>G
  hgvsp: ENSP00000403265.3:p.Ile94Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.137A>G
  hgvsp: ENSP00000456468.1:p.Ile47Val
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.280A>G
  hgvsp: ENSP00000260376.7:p.Ile94Val
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17093
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile94Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

15-72557477-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557477
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557477
    reference: chr 15
allele count: 1
allele frequency: 8.529366609235598e-6
allele num: 117242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.273A>G
  hgvsp: ENST00000260376.7:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1097A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.273A>G
  hgvsp: ENST00000287196.9:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.273A>G
  hgvsp: ENST00000419739.3:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.273A>G
  hgvsp: ENST00000567440.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.273A>G
  hgvsp: ENST00000565443.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.273A>G
  hgvsp: ENST00000569795.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.130A>G
  hgvsp: ENST00000564610.1:c.130A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.131A>G
  hgvsp: ENST00000567974.1:c.131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*143A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.476A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17123
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr91Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

15-72557480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557480
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557480
    reference: chr 15
allele count: 5
allele frequency: 4.271167908152806e-5
allele num: 117064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.270G>A
  hgvsp: ENST00000260376.7:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.270G>A
  hgvsp: ENST00000565443.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.270G>A
  hgvsp: ENST00000569795.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.127G>A
  hgvsp: ENST00000564610.1:c.127G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.473G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1094G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.270G>A
  hgvsp: ENST00000287196.9:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.128G>A
  hgvsp: ENST00000567974.1:c.128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.270G>A
  hgvsp: ENST00000567440.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.270G>A
  hgvsp: ENST00000419739.3:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17049
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29289
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg90Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

15-72557481-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557481
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557481
    reference: chr 15
allele count: 1
allele frequency: 8.551978927923921e-6
allele num: 116932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.269G>C
  hgvsp: ENSP00000456370.1:p.Arg90Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.269G>C
  hgvsp: ENSP00000454298.1:p.Arg90Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.127G>C
  hgvsp: ENSP00000455815.1:p.Arg43Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.269G>C
  hgvsp: ENSP00000403265.3:p.Arg90Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*139G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.269G>C
  hgvsp: ENSP00000456348.1:p.Arg90Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.472G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.269G>C
  hgvsp: ENSP00000260376.7:p.Arg90Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.269G>C
  hgvsp: ENSP00000287196.9:p.Arg90Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.126G>C
  hgvsp: ENSP00000456468.1:p.Arg43Pro
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1093G>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg90Pro
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ

15-72557481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557481
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557481
    reference: chr 15
allele count: 4
allele frequency: 3.420791571169569e-5
allele num: 116932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.269G>A
  hgvsp: ENSP00000260376.7:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.269G>A
  hgvsp: ENSP00000454298.1:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.269G>A
  hgvsp: ENSP00000456370.1:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1093G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.472G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.269G>A
  hgvsp: ENSP00000403265.3:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.127G>A
  hgvsp: ENSP00000455815.1:p.Arg43Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.269G>A
  hgvsp: ENSP00000456348.1:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*139G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.269G>A
  hgvsp: ENSP00000287196.9:p.Arg90Gln
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.126G>A
  hgvsp: ENSP00000456468.1:p.Arg43Gln
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg90Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

15-72557504-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557504
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557504
    reference: chr 15
allele count: 1
allele frequency: 8.847365254627173e-6
allele num: 113028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.246C>G
  hgvsp: ENST00000419739.3:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.449C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.246C>G
  hgvsp: ENST00000565443.1:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.104C>G
  hgvsp: ENST00000567974.1:c.104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.246C>G
  hgvsp: ENST00000569795.1:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.246C>G
  hgvsp: ENST00000567440.1:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1070C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.246C>G
  hgvsp: ENST00000260376.7:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*116C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.246C>G
  hgvsp: ENST00000287196.9:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.103C>G
  hgvsp: ENST00000564610.1:c.103C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val82Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-72557506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557506
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557506
    reference: chr 15
allele count: 1
allele frequency: 8.906464311797502e-6
allele num: 112278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.101G>A
  hgvsp: ENSP00000456468.1:p.Val35Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.244G>A
  hgvsp: ENSP00000260376.7:p.Val82Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.447G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.244G>A
  hgvsp: ENSP00000456348.1:p.Val82Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.244G>A
  hgvsp: ENSP00000456370.1:p.Val82Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.244G>A
  hgvsp: ENSP00000454298.1:p.Val82Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.102G>A
  hgvsp: ENSP00000455815.1:p.Val35Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.244G>A
  hgvsp: ENSP00000403265.3:p.Val82Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1068G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.244G>A
  hgvsp: ENSP00000287196.9:p.Val82Ile
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val82Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-72557516-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557516
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557516
    reference: chr 15
allele count: 1
allele frequency: 9.184254514061094e-6
allele num: 108882
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-4T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-4T>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.238-4T>G
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

15-72557516-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557516
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557513
    reference: chr 15
allele count: 2
allele frequency: 1.836850902812219e-5
allele num: 108882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-7_95-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-7_238-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-7_238-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-7_*108-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-7_238-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-7_96-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-7_238-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-7_238-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-7_441-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-7_1062-5delCTT
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-7_238-5delCTT
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14523
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.238-7_238-5delCTT
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: AAAG
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

15-72557518-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557518
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557518
    reference: chr 15
allele count: 1
allele frequency: 9.259773691130989e-6
allele num: 107994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-6T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-6T>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.238-6T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-72557521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557521
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557521
    reference: chr 15
allele count: 5
allele frequency: 4.65480002979072e-5
allele num: 107416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-9T>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-9T>C
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13588
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

15-72557531-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557531
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557531
    reference: chr 15
allele count: 2
allele frequency: 1.923150890418862e-5
allele num: 103996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-19A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-19A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17882
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

15-72557533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557533
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557533
    reference: chr 15
allele count: 1
allele frequency: 9.689734695064048e-6
allele num: 103202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-21C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-21C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS

15-72557533-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557533
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557533
    reference: chr 15
allele count: 2
allele frequency: 1.93794693901281e-5
allele num: 103202
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-21C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-21C>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

15-72557536-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557536
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557536
    reference: chr 15
allele count: 6
allele frequency: 5.854115443156539e-5
allele num: 102492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-24A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

15-72557545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557545
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557545
    reference: chr 15
allele count: 1
allele frequency: 1.010754427104391e-5
allele num: 98936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-33C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-33C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/15-72557550-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557550
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557550
    reference: chr 15
allele count: 2
allele frequency: 2.082422273588638e-5
allele num: 96042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-38T>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-38T>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18837
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10740
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

15-72557551-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557551
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557551
    reference: chr 15
allele count: 2
allele frequency: 2.095908786049631e-5
allele num: 95424
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-39A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-39A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-72557555-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557555
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557555
    reference: chr 15
allele count: 1
allele frequency: 1.072961373390558e-5
allele num: 93200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-43G>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-43G>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

15-72557555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557555
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557555
    reference: chr 15
allele count: 1
allele frequency: 1.072961373390558e-5
allele num: 93200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-43G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-43G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17841
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

15-72557556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557556
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557556
    reference: chr 15
allele count: 4
allele frequency: 4.406548130521956e-5
allele num: 90774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-44C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-44C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17118
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

15-72557557-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557557
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557557
    reference: chr 15
allele count: 1
allele frequency: 1.09394827812541e-5
allele num: 91412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.238-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.238-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.441-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*108-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.95-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.238-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.238-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.238-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.96-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.238-45T>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1062-45T>A
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10891
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17082
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

15-72557671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557671
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557671
    reference: chr 15
allele count: 9
allele frequency: 7.5642965204236e-5
allele num: 118980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+83G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+83G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11240
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-72557673-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557673
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557673
    reference: chr 15
allele count: 1
allele frequency: 8.428292090890703e-6
allele num: 118648
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*45G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+81G>C
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+81G>C
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11351
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

15-72557673-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557673
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557673
    reference: chr 15
allele count: 1
allele frequency: 8.428292090890703e-6
allele num: 118648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*45G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+81G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+81G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

15-72557679-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557679
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557679
    reference: chr 15
allele count: 1
allele frequency: 8.392359595823962e-6
allele num: 119156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+75G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

15-72557690-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557690
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557690
    reference: chr 15
allele count: 1
allele frequency: 8.368480953337351e-6
allele num: 119496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*28C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+64C>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+64C>G
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

15-72557695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557695
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557695
    reference: chr 15
allele count: 8
allele frequency: 6.68002672010688e-5
allele num: 119760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*23G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+59G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+59G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13304
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20390
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

15-72557698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557698
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557698
    reference: chr 15
allele count: 1
allele frequency: 8.342927700188551e-6
allele num: 119862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+56C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+56C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

15-72557730-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557730
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557730
    reference: chr 15
allele count: 29
allele frequency: 2.403049386808087e-4
allele num: 120680
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.218A>G
  hgvsp: ENST00000565999.1:c.218A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+24A>G
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+24A>G
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln73Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-72557737-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557737
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557737
    reference: chr 15
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.211C>T
  hgvsp: ENSP00000457134.1:p.Thr71Ile
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+17C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+17C>T
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr71Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

15-72557747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557747
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557747
    reference: chr 15
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.237+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.95+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.237+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.94+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.237+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1061+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.237+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.440+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.237+7G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.201G>A
  hgvsp: ENSP00000457134.1:p.Gly68Arg
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.237+7G>A
  variant of: http://identifiers.org/hgnc/26921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly68Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

15-72557756-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557756
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557756
    reference: chr 15
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.235G>A
  hgvsp: ENSP00000403265.3:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.192G>A
  hgvsp: ENSP00000457134.1:p.Asp65Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.92G>A
  hgvsp: ENSP00000456468.1:p.Asp32Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1059G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.235G>A
  hgvsp: ENSP00000260376.7:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.235G>A
  hgvsp: ENSP00000454298.1:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.93G>A
  hgvsp: ENSP00000455815.1:p.Asp32Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.235G>A
  hgvsp: ENSP00000456370.1:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.438G>A
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.235G>A
  hgvsp: ENSP00000287196.9:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.235G>A
  hgvsp: ENSP00000456348.1:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp79Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

15-72557757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72557757
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 72557757
    reference: chr 15
allele count: 6
allele frequency: 4.969108707534825e-5
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456348
  ensembl transcript: ENST00000569795
  gene symbol: PARP6
  hgvsc: ENST00000569795.1:c.234C>T
  hgvsp: ENST00000569795.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000403265
  ensembl transcript: ENST00000419739
  gene symbol: PARP6
  hgvsc: ENST00000419739.3:c.234C>T
  hgvsp: ENST00000419739.3:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000454298
  ensembl transcript: ENST00000567440
  gene symbol: PARP6
  hgvsc: ENST00000567440.1:c.234C>T
  hgvsp: ENST00000567440.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000457134
  ensembl transcript: ENST00000565999
  gene symbol: PARP6
  hgvsc: ENST00000565999.1:c.191C>T
  hgvsp: ENST00000565999.1:c.191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456370
  ensembl transcript: ENST00000565443
  gene symbol: PARP6
  hgvsc: ENST00000565443.1:c.234C>T
  hgvsp: ENST00000565443.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000413097
  gene symbol: PARP6
  hgvsc: ENST00000413097.2:n.1058C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000260376
  ensembl transcript: ENST00000260376
  gene symbol: PARP6
  hgvsc: ENST00000260376.7:c.234C>T
  hgvsp: ENST00000260376.7:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000287196
  ensembl transcript: ENST00000287196
  gene symbol: PARP6
  hgvsc: ENST00000287196.9:c.234C>T
  hgvsp: ENST00000287196.9:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137817
  ensembl transcript: ENST00000544520
  gene symbol: PARP6
  hgvsc: ENST00000544520.1:n.437C>T
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000455815
  ensembl transcript: ENST00000567974
  gene symbol: PARP6
  hgvsc: ENST00000567974.1:c.92C>T
  hgvsp: ENST00000567974.1:c.92C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137817
  ensembl protein: ENSP00000456468
  ensembl transcript: ENST00000564610
  gene symbol: PARP6
  hgvsc: ENST00000564610.1:c.91C>T
  hgvsp: ENST00000564610.1:c.91C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu78Leu
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 709
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14615
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20614
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2202
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6408
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
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: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.139999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

FS
type: SiteQuality
SIO_000300: 7.74e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 2.436955e6

QD
type: SiteQuality
SIO_000300: 1.199e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.559e0

GenotypeDepth
all individuals: 2912
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2201
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14599
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4502
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20614
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4997
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.736e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 1.542e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 2.436942e6

GenotypeDepth
all individuals: 564
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 14616
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4500
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20615
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4999
bin: 7.75e1
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: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

VQSLOD
type: SiteQuality
SIO_000300: 8.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.56e-1

DP
type: SiteQuality
SIO_000300: 2.436847e6

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

QD
type: SiteQuality
SIO_000300: 1.646e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeDepth
all individuals: 708
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12446
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20613
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4995
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4499
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6407
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.204e0

QD
type: SiteQuality
SIO_000300: 1.305e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.436677e6

GenotypeDepth
all individuals: 1215
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4499
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14624
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20611
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

DP
type: SiteQuality
SIO_000300: 2.436601e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.409e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.16e0

QD
type: SiteQuality
SIO_000300: 1.44e1

GenotypeDepth
all individuals: 1701
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6407
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 14625
bin: 6.25e1
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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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variant carriers: 0

East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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Latino
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allele num: 11568
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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African
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

South Asian
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European (Non-Finnish)
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allele num: 66706
num of homozygotes: 0

African
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Latino
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BaseQRankSum
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SIO_000300: -1.111e0

InbreedingCoeff
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VQSLOD
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FS
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DP
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MQ
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

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

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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allele num: 8622
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African
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European (Finnish)
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Latino
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num of homozygotes: 0

Other
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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Other
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East Asian
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FS
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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allele num: 9786
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Other
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European (Non-Finnish)
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East Asian
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Latino
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QD
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FS
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MQRankSum
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DP
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.702783867383405e-4
allele num: 66598
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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South Asian
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African
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European (Finnish)
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allele frequency: 2.419842710223836e-3
allele num: 6612
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

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

East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66562
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South Asian
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Other
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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FS
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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allele num: 66408
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African
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East Asian
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South Asian
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BaseQRankSum
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FS
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DP
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QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

GenotypeQuality
all individuals: 4120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.238971302714258e-5
allele num: 61748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.325095e6

MQ
type: SiteQuality
SIO_000300: 5.892e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
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SIO_000300: -1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

FS
type: SiteQuality
SIO_000300: 6.24e0

VQSLOD
type: SiteQuality
SIO_000300: -6.594e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
all individuals: 285
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 4318
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.56254101588135e-5
allele num: 15238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8750
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.33423e6

MQ
type: SiteQuality
SIO_000300: 5.904e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2835
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4775
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.31250820317627e-4
allele num: 15238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62106
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.127e0

DP
type: SiteQuality
SIO_000300: 1.340252e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 9.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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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: 1545
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.602410024677114e-4
allele num: 62406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8070
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.362561e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.477e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 22

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8822
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

South Asian
type: Population
allele count: 23
allele frequency: 1.495254193212846e-3
allele num: 15382
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.014e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.407774e6

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.130965844831486e-4
allele num: 8842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10410
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
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QD
type: SiteQuality
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MQ
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DP
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575398575839688e-5
allele num: 63476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.638e-1

ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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FS
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BaseQRankSum
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MQ
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QD
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SIO_000300: 9.1e0

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

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 9.75e1
variant carriers: 13

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63752
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.352569882777277e-3
allele num: 8872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.196172248803828e-3
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.459972e6

QD
type: SiteQuality
SIO_000300: 1.329e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.632e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

GenotypeDepth
all individuals: 236
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4786
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.547121752419766e-4
allele num: 15704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 1.1718e1

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.512081e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.253e0

QD
type: SiteQuality
SIO_000300: 1.393e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

GenotypeDepth
all individuals: 20
bin: 9.25e1
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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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 761
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GenotypeQuality
all individuals: 1571
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539456264047538e-5
allele num: 64958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.514389e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

MQRankSum
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SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.311e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
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GenotypeQuality
all individuals: 287
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 42728
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2825
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 419
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1038
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variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.611411706837186e-5
allele num: 65056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15732
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.517235e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

FS
type: SiteQuality
SIO_000300: 6.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.309e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 7.68e-1

GenotypeDepth
all individuals: 123
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15648
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2307
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variant carriers: 0

GenotypeQuality
all individuals: 214
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variant carriers: 0

GenotypeQuality
all individuals: 399
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GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 443
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GenotypeQuality
all individuals: 158
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1438
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 42929
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535343609899896e-5
allele num: 65132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.518922e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 3.09e0

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ClippingRankSum
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QD
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SIO_000300: 1.644e1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.41e-1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 156
bin: 4.75e1
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GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15944
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.563154052080798e-5
allele num: 65744
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.79e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.866e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

GenotypeDepth
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bin: 9.25e1
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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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2822
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 237
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15960
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.5220700152207e-4
allele num: 6570
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.275e1

MQ
type: SiteQuality
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FS
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: 2.64e0

ReadPosRankSum
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GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 56
bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 288
bin: 5.25e1
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GenotypeQuality
all individuals: 2826
bin: 9.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52494815176284e-5
allele num: 65576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.710516805204192e-4
allele num: 11068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

ClippingRankSum
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SIO_000300: 1.07e0

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.049e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

DP
type: SiteQuality
SIO_000300: 1.540674e6

GenotypeDepth
all individuals: 70
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 59
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529519730804527e-5
allele num: 65380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11010
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9074
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: -4.14e-1

FS
type: SiteQuality
SIO_000300: 1.111e0

MQRankSum
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SIO_000300: 2.56e-1

BaseQRankSum
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SIO_000300: -1.194e0

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.140000000000001e0

DP
type: SiteQuality
SIO_000300: 1.534091e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.658375199117755e-5
allele num: 65288
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15806
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9066
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

QD
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SIO_000300: 1.236e1

VQSLOD
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SIO_000300: 1.51e0

FS
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SIO_000300: 2.67e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -4.0e-4

ClippingRankSum
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SIO_000300: -2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 1.531973e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.567e0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1524
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533507130808158e-5
allele num: 65210
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15786
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.71e-1

FS
type: SiteQuality
SIO_000300: 1.264e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

InbreedingCoeff
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SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
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SIO_000300: 1.531244e6

VQSLOD
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SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 1.341e1

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.25e1
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GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15786
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.518648838845883e-4
allele num: 8526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533507130808158e-5
allele num: 65210
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.264e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

MQRankSum
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SIO_000300: 2.86e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: -3.71e-1

InbreedingCoeff
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.531244e6

QD
type: SiteQuality
SIO_000300: 1.341e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeDepth
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variant carriers: 0

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
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63080
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 6.521455588887439e-5
allele num: 15334
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.955e1

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

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

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
all individuals: 565
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15006
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.15233924867481e-4
allele num: 8678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

FS
type: SiteQuality
SIO_000300: 6.01e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

MQ
type: SiteQuality
SIO_000300: 5.705e1

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

DP
type: SiteQuality
SIO_000300: 1.359466e6

GenotypeDepth
all individuals: 58
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1692
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.298479400996141e-5
allele num: 60634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

FS
type: SiteQuality
SIO_000300: 6.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.705e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

DP
type: SiteQuality
SIO_000300: 1.359466e6

QD
type: SiteQuality
SIO_000300: 1.173e1

GenotypeDepth
all individuals: 58
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3859
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14938
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.622849724115547e-4
allele num: 6162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.336306e6

QD
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: -8.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 3.501e0

MQRankSum
type: SiteQuality
SIO_000300: -1.045e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
all individuals: 1195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 441
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 1372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14892
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.357011532675916e-5
allele num: 59830
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.3207e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

QD
type: SiteQuality
SIO_000300: 1.414e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.024e0

FS
type: SiteQuality
SIO_000300: 3.635e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

GenotypeQuality
all individuals: 1019
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4856
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2487
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4096
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16922
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.456141563558443e-5
allele num: 57868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 1.904e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 1.215953e6

VQSLOD
type: SiteQuality
SIO_000300: -3.38e-1

QD
type: SiteQuality
SIO_000300: 1.975e1

GenotypeQuality
all individuals: 360
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 412
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variant carriers: 0

GenotypeQuality
all individuals: 1300
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GenotypeQuality
all individuals: 1119
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4325
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8758
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14554
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.346257404415724e-4
allele num: 7428
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

QD
type: SiteQuality
SIO_000300: 1.511e1

DP
type: SiteQuality
SIO_000300: 1.197996e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 2804
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 606
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8758
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.388344877000239e-4
allele num: 8374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14554
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-3

QD
type: SiteQuality
SIO_000300: 1.511e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 1.197996e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.72e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2804
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 14859
bin: 6.25e1
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GenotypeQuality
all individuals: 1297
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GenotypeQuality
all individuals: 5618
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.143646408839779e-4
allele num: 14480
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 4.17e0

MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.320000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

FS
type: SiteQuality
SIO_000300: 5.445e0

DP
type: SiteQuality
SIO_000300: 1.179496e6

QD
type: SiteQuality
SIO_000300: 1.565e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7078
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.820167455405897e-5
allele num: 54940
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14170
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -6.1e-3

QD
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DP
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
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SIO_000300: -3.349e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 13930
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.755586434821797e-5
allele num: 53254
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6880
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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MQRankSum
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SIO_000300: -3.8e-1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

DP
type: SiteQuality
SIO_000300: 1.078719e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.25344697919278e-4
allele num: 7978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52890
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.198387561186294e-5
allele num: 13892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5594
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.252e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.809e0

DP
type: SiteQuality
SIO_000300: 1.073395e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13754
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6652
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.939487975174554e-5
allele num: 51560
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13754
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.503307276007216e-4
allele num: 6652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.181e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5352
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 7.973527887413786e-5
allele num: 50166
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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

Latino
type: Population
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allele frequency: 1.447596988998263e-4
allele num: 6908
num of homozygotes: 0

Other
type: Population
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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MQ
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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African
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allele frequency: 9.284093253558903e-4
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Latino
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VQSLOD
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ClippingRankSum
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FS
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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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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.89521437466643e-5
allele num: 11242
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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FS
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MQ
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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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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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East Asian
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Other
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Latino
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.513867021920794e-5
allele num: 66056
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European (Finnish)
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Latino
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South Asian
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

South Asian
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allele num: 16276
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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VQSLOD
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DP
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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African
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Latino
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 888
num of homozygotes: 0

Latino
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South Asian
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.347826086956522e-4
allele num: 66700
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 16490
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.981434e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.408e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7928
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25186
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12576
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.204e0

MQRankSum
type: SiteQuality
SIO_000300: -7.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e-1

QD
type: SiteQuality
SIO_000300: 1.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

FS
type: SiteQuality
SIO_000300: 4.933e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.981093e6

GenotypeDepth
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1144
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12576
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3184
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25216
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4283
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7940
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 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: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 1.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.88e-1

DP
type: SiteQuality
SIO_000300: 1.981714e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

FS
type: SiteQuality
SIO_000300: 4.116e0

MQ
type: SiteQuality
SIO_000300: 5.755e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.802e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeDepth
all individuals: 4527
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12576
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25217
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3180
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4283
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.982011e6

QD
type: SiteQuality
SIO_000300: 1.322e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 6.423e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.11e-1

GenotypeDepth
all individuals: 490
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 673
bin: 6.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3397
bin: 7.25e1
variant carriers: 0

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

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

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