15-85632691-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85632691
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85632691
    reference: chr 15
allele count: 1
allele frequency: 1.397780324844148e-5
allele num: 71542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-1584C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.714+44C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.714+44C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+44C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+5816C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+5816C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+5816C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.498+44C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+5816C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.714+44C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

15-85632697-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85632697
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85632697
    reference: chr 15
allele count: 1
allele frequency: 1.394777951350145e-5
allele num: 71696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.714+50C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+5822C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.714+50C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+50C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.714+50C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+5822C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+5822C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+5822C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.498+50C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-1578C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17489
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12785
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

15-85633920-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85633920
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85633921
    reference: chr 15
allele count: 2
allele frequency: 3.522367030644593e-4
allele num: 5678
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.715-23dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-349dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-349dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-349dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7051dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+7051dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+7051dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7051dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1279dupC
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-349dupC
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

15-85633934-CCCCCATCTAAACAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85633934
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85633920
    reference: chr 15
allele count: 1
allele frequency: 1.314060446780552e-4
allele num: 7610
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9635
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1869
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
hgvs: c.715-11_717delCATCTAAACAGCCC
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: CCCCCATCTAAACAG
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-85633938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85633938
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85633938
    reference: chr 15
allele count: 1
allele frequency: 1.204819277108434e-4
allele num: 8300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1291C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.715-11C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-337C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+7063C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7063C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+7063C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7063C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-337C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-337C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-337C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS

15-85633949-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85633949
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85633949
    reference: chr 15
allele count: 19
allele frequency: 1.979991663192997e-3
allele num: 9596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7074C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1302C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-326C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+7074C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-326C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+7074C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-326C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7074C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.715C>T
  hgvsp: ENSP00000431976.1:p.Pro239Ser
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-326C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10575
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro239Ser
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-85633965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85633965
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85633965
    reference: chr 15
allele count: 1
allele frequency: 9.574875526618154e-5
allele num: 10444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-310C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.731C>T
  hgvsp: ENSP00000431976.1:p.Ser244Phe
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-310C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-310C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1318C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7090C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+7090C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-310C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+7090C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7090C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser244Phe
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

15-85633966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85633966
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85633966
    reference: chr 15
allele count: 1
allele frequency: 9.547450830628223e-5
allele num: 10474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7091C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.635+7091C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-309C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7091C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2322+7091C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-309C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1319C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.732C>T
  hgvsp: ENST00000485596.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-309C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-309C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser244Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

15-85634064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634064
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634064
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 10700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7189A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*11A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-211A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-211A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7189A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-7115A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-211A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1417A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-211A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-7115A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14492
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

15-85634067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634067
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634067
    reference: chr 15
allele count: 1
allele frequency: 9.402030838661151e-5
allele num: 10636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-7112C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7192C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-208C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-208C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*14C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-208C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1420C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-208C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-7112C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7192C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-85634228-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634228
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634228
    reference: chr 15
allele count: 1
allele frequency: 9.216419973825367e-6
allele num: 108502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*94-47A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7353A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-47A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6951A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-47A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6951A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7353A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-47A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-47A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1581A>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12188
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5303
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

15-85634230-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634230
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634230
    reference: chr 15
allele count: 1
allele frequency: 9.200139842125601e-6
allele num: 108694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6949A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6949A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7355A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1583A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-45A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-45A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-45A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-45A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*94-45A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7355A>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14533
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

15-85634237-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634237
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634237
    reference: chr 15
allele count: 1
allele frequency: 9.147959090326949e-6
allele num: 109314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1590T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7362T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-38T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6942T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-38T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*94-38T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6942T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7362T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-38T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-38T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20603
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5683
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

15-85634263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634263
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634263
    reference: chr 15
allele count: 1
allele frequency: 8.613857974709713e-6
allele num: 116092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1616G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*94-12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7388G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6916G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6916G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7388G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-12G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5200
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

15-85634274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634274
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634274
    reference: chr 15
allele count: 1
allele frequency: 8.418217021634817e-6
allele num: 118790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*94-1G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6905G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7399G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.499-1G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7399G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1627G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.715-1G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.715-1G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.636-1G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6905G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
hgvs: c.715-1G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

15-85634297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634297
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634297
    reference: chr 15
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*116C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6882C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.521C>T
  hgvsp: ENSP00000453808.1:p.Thr174Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.658C>T
  hgvsp: ENSP00000432309.1:p.Gln220Ter
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1650C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7422C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.737C>T
  hgvsp: ENSP00000311453.4:p.Thr246Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.737C>T
  hgvsp: ENSP00000378056.1:p.Thr246Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6882C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7422C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln220Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

15-85634302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634302
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634302
    reference: chr 15
allele count: 6
allele frequency: 4.974629390110437e-5
allele num: 120612
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.742A>G
  hgvsp: ENSP00000311453.4:p.Met248Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7427A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*121A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.742A>G
  hgvsp: ENSP00000378056.1:p.Met248Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6877A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6877A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.526A>G
  hgvsp: ENSP00000453808.1:p.Met176Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1655A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7427A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.663A>G
  hgvsp: ENST00000478717.1:c.663A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38261
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met248Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-85634308-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634308
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634308
    reference: chr 15
allele count: 16
allele frequency: 1.324920090757026e-4
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.748T>A
  hgvsp: ENSP00000311453.4:p.Tyr250Asn
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*127T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6871T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6871T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7433T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7433T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.748T>A
  hgvsp: ENSP00000378056.1:p.Tyr250Asn
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.532T>A
  hgvsp: ENSP00000453808.1:p.Tyr178Asn
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.669T>A
  hgvsp: ENST00000478717.1:c.669T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1661T>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr250Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

15-85634308-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634308
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634308
    reference: chr 15
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.748T>C
  hgvsp: ENSP00000311453.4:p.Tyr250His
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*127T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.532T>C
  hgvsp: ENSP00000453808.1:p.Tyr178His
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7433T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6871T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.669T>C
  hgvsp: ENST00000478717.1:c.669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.748T>C
  hgvsp: ENSP00000378056.1:p.Tyr250His
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6871T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1661T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7433T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr250His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/15-85634311-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634311
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634311
    reference: chr 15
allele count: 3
allele frequency: 2.483608185972581e-5
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7436C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*130C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.535C>A
  hgvsp: ENSP00000453808.1:p.Gln179Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1664C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6868C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.751C>A
  hgvsp: ENSP00000378056.1:p.Gln251Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.672C>A
  hgvsp: ENST00000478717.1:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.751C>A
  hgvsp: ENSP00000311453.4:p.Gln251Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7436C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6868C>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln251Lys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

15-85634318-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634318
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634318
    reference: chr 15
allele count: 4
allele frequency: 3.310216984723349e-5
allele num: 120838
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.758G>T
  hgvsp: ENSP00000311453.4:p.Gly253Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.679G>T
  hgvsp: ENSP00000432309.1:p.Val227Leu
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7443G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.542G>T
  hgvsp: ENSP00000453808.1:p.Gly181Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*137G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6861G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.758G>T
  hgvsp: ENSP00000378056.1:p.Gly253Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1671G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6861G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7443G>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly253Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

15-85634326-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634326
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634326
    reference: chr 15
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1679A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7451A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7451A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.766A>G
  hgvsp: ENSP00000378056.1:p.Ile256Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*145A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.766A>G
  hgvsp: ENSP00000311453.4:p.Ile256Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6853A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.687A>G
  hgvsp: ENST00000478717.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.550A>G
  hgvsp: ENSP00000453808.1:p.Ile184Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6853A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile256Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

15-85634329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634329
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634329
    reference: chr 15
allele count: 3
allele frequency: 2.481759070829404e-5
allele num: 120882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6850G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.553G>A
  hgvsp: ENSP00000453808.1:p.Gly185Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6850G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*148G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7454G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1682G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7454G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.769G>A
  hgvsp: ENSP00000311453.4:p.Gly257Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.769G>A
  hgvsp: ENSP00000378056.1:p.Gly257Arg
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly257Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

15-85634337-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634337
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634337
    reference: chr 15
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6842G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6842G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*11G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*156G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.777G>T
  hgvsp: ENSP00000378056.1:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7462G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.561G>T
  hgvsp: ENSP00000453808.1:p.Glu187Asp
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1690G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7462G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.777G>T
  hgvsp: ENSP00000311453.4:p.Glu259Asp
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu259Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-85634349-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634349
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634349
    reference: chr 15
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*23G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6830G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*168G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.573G>T
  hgvsp: ENST00000557957.1:c.573G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7474G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1702G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7474G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6830G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.789G>T
  hgvsp: ENST00000310298.4:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.789G>T
  hgvsp: ENST00000394553.1:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val263Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

15-85634357-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634357
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634357
    reference: chr 15
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*176A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.581A>T
  hgvsp: ENSP00000453808.1:p.Asn194Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6822A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1710A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.797A>T
  hgvsp: ENSP00000378056.1:p.Asn266Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7482A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7482A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6822A>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.797A>T
  hgvsp: ENSP00000311453.4:p.Asn266Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*31A>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn266Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

15-85634368-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634368
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634368
    reference: chr 15
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1721G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6811G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7493G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.808G>T
  hgvsp: ENSP00000311453.4:p.Ala270Ser
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*187G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.808G>T
  hgvsp: ENSP00000378056.1:p.Ala270Ser
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6811G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7493G>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.592G>T
  hgvsp: ENSP00000453808.1:p.Ala198Ser
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala270Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

15-85634379-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634379
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634379
    reference: chr 15
allele count: 1
allele frequency: 8.307717869901138e-6
allele num: 120370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*53C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6800C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*198C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.819C>G
  hgvsp: ENST00000394553.1:c.819C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7504C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.819C>G
  hgvsp: ENST00000310298.4:c.819C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7504C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6800C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.603C>G
  hgvsp: ENST00000557957.1:c.603C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1732C>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40640
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu273Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

15-85634379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634379
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634379
    reference: chr 15
allele count: 2
allele frequency: 1.661543573980228e-5
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.819C>T
  hgvsp: ENST00000310298.4:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.819C>T
  hgvsp: ENST00000394553.1:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7504C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6800C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.603C>T
  hgvsp: ENST00000557957.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*53C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7504C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*198C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6800C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1732C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu273Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

15-85634380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634380
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634380
    reference: chr 15
allele count: 6
allele frequency: 4.986536351850005e-5
allele num: 120324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6799G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7505G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.820G>A
  hgvsp: ENSP00000311453.4:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*54G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.604G>A
  hgvsp: ENSP00000453808.1:p.Asp202Asn
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1733G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.820G>A
  hgvsp: ENSP00000378056.1:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7505G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6799G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40618
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp274Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

15-85634386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634386
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634386
    reference: chr 15
allele count: 2
allele frequency: 1.665972511453561e-5
allele num: 120050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6793A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*205A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7511A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.826A>G
  hgvsp: ENSP00000378056.1:p.Ile276Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6793A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.826A>G
  hgvsp: ENSP00000311453.4:p.Ile276Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.610A>G
  hgvsp: ENSP00000453808.1:p.Ile204Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*60A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7511A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1739A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile276Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

15-85634398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634398
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634398
    reference: chr 15
allele count: 1
allele frequency: 8.398421096833796e-6
allele num: 119070
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.838A>G
  hgvsp: ENSP00000311453.4:p.Ile280Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1751A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6781A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7523A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.838A>G
  hgvsp: ENSP00000378056.1:p.Ile280Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*72A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*217A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6781A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.622A>G
  hgvsp: ENSP00000453808.1:p.Ile208Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7523A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5345
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile280Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-85634403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634403
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634403
    reference: chr 15
allele count: 1
allele frequency: 8.435686327439601e-6
allele num: 118544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*222G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.843G>A
  hgvsp: ENST00000394553.1:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6776G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*77G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1756G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.843G>A
  hgvsp: ENST00000310298.4:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.627G>A
  hgvsp: ENST00000557957.1:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6776G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7528G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7528G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12703
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5344
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg281Arg
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

15-85634421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634421
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634421
    reference: chr 15
allele count: 1
allele frequency: 8.56971462850287e-6
allele num: 116690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7546G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6758G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+9G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1774G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+9G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6758G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+9G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+9G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7546G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+9G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-85634424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634424
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634424
    reference: chr 15
allele count: 1
allele frequency: 8.585164835164835e-6
allele num: 116480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7549G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6755G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7549G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6755G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+12G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1777G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+12G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

15-85634431-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634431
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634431
    reference: chr 15
allele count: 1
allele frequency: 8.651566798747254e-6
allele num: 115586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6748C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7556C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1784C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7556C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+19C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6748C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+19C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+19C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+19C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+19C>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

15-85634435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634435
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634435
    reference: chr 15
allele count: 1
allele frequency: 8.674230595746157e-6
allele num: 115284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+23T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+23T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+23T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1788T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7560T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6744T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6744T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7560T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+23T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+23T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum

15-85634441-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634441
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634440
    reference: chr 15
allele count: 1
allele frequency: 8.728136019271725e-6
allele num: 114572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+32delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6735delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6735delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+32delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+32delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+32delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+32delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7569delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1797delT
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7569delT
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: CT
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-85634449-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634449
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634449
    reference: chr 15
allele count: 1
allele frequency: 8.814921899791968e-6
allele num: 113444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7574A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+37A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+37A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+37A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1802A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+37A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+37A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6730A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6730A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7574A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

15-85634452-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634452
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634450
    reference: chr 15
allele count: 2
allele frequency: 1.768721921539496e-5
allele num: 113076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6721_2323-6720delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+46_636+47delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+46_*231+47delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+46_852+47delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7583_*79+7584delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1811_714+1812delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+46_852+47delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6721_636-6720delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+46_*86+47delGA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7583_378+7584delGA
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5343
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: CAG
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-85634454-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85634454
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85634454
    reference: chr 15
allele count: 2
allele frequency: 1.772326887971218e-5
allele num: 112846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-6725G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.636+42G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*86+42G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*79+7579G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.852+42G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.378+7579G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.714+1807G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*231+42G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-6725G>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.852+42G>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9966
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6221
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3725
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

15-85641139-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641139
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641139
    reference: chr 15
allele count: 1
allele frequency: 9.079353550027237e-6
allele num: 110140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2107T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11145T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.106T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-40T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-40T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  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: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-85641144-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641144
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641144
    reference: chr 15
allele count: 2
allele frequency: 1.812415043044857e-5
allele num: 110350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.111C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2102C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11140C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-35C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-35C>G
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24384
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-85641145-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641145
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641145
    reference: chr 15
allele count: 4
allele frequency: 3.613891800079506e-5
allele num: 110684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.112A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2101A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-34A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11139A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-34A>C
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9055
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10403
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25084
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

15-85641156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641156
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641156
    reference: chr 15
allele count: 7
allele frequency: 6.211510816902408e-5
allele num: 112694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.123C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2090C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11128C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-23C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-23C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10804
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

15-85641157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641157
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641157
    reference: chr 15
allele count: 9
allele frequency: 7.945476375450243e-5
allele num: 113272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2089G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11127G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.124G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-22G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-22G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32540
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

15-85641163-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641163
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641164
    reference: chr 15
allele count: 1
allele frequency: 8.700494188069882e-6
allele num: 114936
alternate allele: TA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.131dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2082dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11120dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-15dupA
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-15dupA
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  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: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

15-85641166-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641166
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641166
    reference: chr 15
allele count: 3
allele frequency: 2.594168309639929e-5
allele num: 115644
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-13A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11118A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.133A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2080A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-13A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-85641168-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641168
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641168
    reference: chr 15
allele count: 1
allele frequency: 8.620392400262059e-6
allele num: 116004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11116T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2078T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.135T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-11T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-11T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

15-85641169-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641169
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641169
    reference: chr 15
allele count: 1
allele frequency: 8.610594475442584e-6
allele num: 116136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.136C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11115C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2077C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-10C>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-10C>G
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

15-85641176-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641176
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641176
    reference: chr 15
allele count: 1
allele frequency: 8.523405270873819e-6
allele num: 117324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.715-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*87-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.637-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.636-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2323-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11108T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.853-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.853-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*232-3T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2070T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.143T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.853-3T>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-85641188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641188
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641188
    reference: chr 15
allele count: 1
allele frequency: 8.417933565668301e-6
allele num: 118794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.862G>A
  hgvsp: ENSP00000378056.1:p.Gly288Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.724G>A
  hgvsp: ENSP00000340679.5:p.Gly242Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.645G>A
  hgvsp: ENST00000559742.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.862G>A
  hgvsp: ENSP00000311453.4:p.Gly288Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.155G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.646G>A
  hgvsp: ENSP00000453808.1:p.Gly216Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2058G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*241G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2332G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11096G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*96G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly288Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

15-85641193-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641193
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641193
    reference: chr 15
allele count: 1
allele frequency: 8.391937026904549e-6
allele num: 119162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.650T>A
  hgvsp: ENSP00000452907.1:p.Phe217Tyr
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.729T>A
  hgvsp: ENST00000339708.5:c.729T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2053T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.160T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.651T>A
  hgvsp: ENST00000557957.1:c.651T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2337T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11091T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*101T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.867T>A
  hgvsp: ENST00000394553.1:c.867T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*246T>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.867T>A
  hgvsp: ENST00000310298.4:c.867T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe217Tyr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

15-85641199-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641199
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641199
    reference: chr 15
allele count: 1
allele frequency: 8.369601606963508e-6
allele num: 119480
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*107T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.873T>C
  hgvsp: ENST00000310298.4:c.873T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.873T>C
  hgvsp: ENST00000394553.1:c.873T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*252T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2047T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2343T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11085T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.166T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.657T>C
  hgvsp: ENST00000557957.1:c.657T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.656T>C
  hgvsp: ENSP00000452907.1:p.Met219Thr
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.735T>C
  hgvsp: ENST00000339708.5:c.735T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13401
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met219Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-85641205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641205
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641205
    reference: chr 15
allele count: 1
allele frequency: 8.359806052499582e-6
allele num: 119620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*113A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2041A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.662A>G
  hgvsp: ENSP00000452907.1:p.Lys221Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.879A>G
  hgvsp: ENST00000394553.1:c.879A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*258A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.663A>G
  hgvsp: ENST00000557957.1:c.663A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2349A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.741A>G
  hgvsp: ENST00000339708.5:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11079A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.172A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.879A>G
  hgvsp: ENST00000310298.4:c.879A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys221Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

15-85641210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641210
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641210
    reference: chr 15
allele count: 1
allele frequency: 8.357989402069439e-6
allele num: 119646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2354A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.668A>G
  hgvsp: ENSP00000453808.1:p.Lys223Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.884A>G
  hgvsp: ENSP00000378056.1:p.Lys295Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*118A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.746A>G
  hgvsp: ENSP00000340679.5:p.Lys249Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.667A>G
  hgvsp: ENSP00000452907.1:p.Lys223Glu
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2036A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*263A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.884A>G
  hgvsp: ENSP00000311453.4:p.Lys295Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11074A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.177A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys295Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

15-85641214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641214
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641214
    reference: chr 15
allele count: 7
allele frequency: 5.851668561492677e-5
allele num: 119624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2358C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.181C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.888C>T
  hgvsp: ENST00000310298.4:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.750C>T
  hgvsp: ENST00000339708.5:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*267C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.672C>T
  hgvsp: ENST00000557957.1:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.888C>T
  hgvsp: ENST00000394553.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*122C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11070C>T
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.671C>T
  hgvsp: ENSP00000452907.1:p.Thr224Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2032C>T
  variant of: http://identifiers.org/hgnc/8793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38331
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr224Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

15-85641215-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641215
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641215
    reference: chr 15
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*123G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.889G>A
  hgvsp: ENSP00000311453.4:p.Gly297Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.751G>A
  hgvsp: ENSP00000340679.5:p.Gly251Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*268G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2359G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.673G>A
  hgvsp: ENSP00000453808.1:p.Gly225Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2031G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.672G>A
  hgvsp: ENST00000559742.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11069G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.889G>A
  hgvsp: ENSP00000378056.1:p.Gly297Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.182G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly297Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

15-85641224-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641224
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641224
    reference: chr 15
allele count: 2
allele frequency: 1.674789395233549e-5
allele num: 119418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.681A>G
  hgvsp: ENSP00000452907.1:p.Ile227Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*277A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.682A>G
  hgvsp: ENSP00000453808.1:p.Ile228Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11060A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.898A>G
  hgvsp: ENSP00000311453.4:p.Ile300Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.760A>G
  hgvsp: ENSP00000340679.5:p.Ile254Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.191A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.898A>G
  hgvsp: ENSP00000378056.1:p.Ile300Val
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2022A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2368A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*132A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13841
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile300Val
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: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-85641230-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641230
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641230
    reference: chr 15
allele count: 1
allele frequency: 8.384056877441857e-6
allele num: 119274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2016C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.766C>A
  hgvsp: ENSP00000340679.5:p.Gln256Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.904C>A
  hgvsp: ENSP00000378056.1:p.Gln302Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2374C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.688C>A
  hgvsp: ENSP00000453808.1:p.Gln230Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.687C>A
  hgvsp: ENSP00000452907.1:p.Asn229Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*283C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.904C>A
  hgvsp: ENSP00000311453.4:p.Gln302Lys
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.197C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11054C>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*138C>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln302Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

15-85641235-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641235
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641236
    reference: chr 15
allele count: 1
allele frequency: 8.39602364320258e-6
allele num: 119104
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.203dupG
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*289dupG
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.910dupG
  hgvsp: ENSP00000378056.1:p.Val304GlyfsTer14
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*144dupG
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.910dupG
  hgvsp: ENSP00000311453.4:p.Val304GlyfsTer14
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11048dupG
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2380dupG
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.772dupG
  hgvsp: ENSP00000340679.5:p.Val258GlyfsTer14
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.693dupG
  hgvsp: ENSP00000452907.1:p.Ter232ValfsTer527
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.694dupG
  hgvsp: ENSP00000453808.1:p.Val232GlyfsTer14
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2010dupG
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val304GlyfsTer14
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

15-85641236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641236
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641236
    reference: chr 15
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2380G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.910G>A
  hgvsp: ENSP00000378056.1:p.Val304Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*289G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.693G>A
  hgvsp: ENSP00000452907.1:p.Met231Ile
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.694G>A
  hgvsp: ENSP00000453808.1:p.Val232Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2010G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.772G>A
  hgvsp: ENSP00000340679.5:p.Val258Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.203G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11048G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.910G>A
  hgvsp: ENSP00000311453.4:p.Val304Met
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val304Met
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/15-85641240-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641240
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641240
    reference: chr 15
allele count: 2
allele frequency: 1.682878395207162e-5
allele num: 118844
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.914A>C
  hgvsp: ENSP00000311453.4:p.Lys305Thr
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.207A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.914A>C
  hgvsp: ENSP00000378056.1:p.Lys305Thr
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11044A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2006A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2384A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*1A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*293A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.698A>C
  hgvsp: ENSP00000453808.1:p.Lys233Thr
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.776A>C
  hgvsp: ENSP00000340679.5:p.Lys259Thr
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*148A>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys305Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/15-85641242-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641242
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641242
    reference: chr 15
allele count: 9
allele frequency: 7.585462881801632e-5
allele num: 118648
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.209A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2386A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*3A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.778A>C
  hgvsp: ENSP00000340679.5:p.Ile260Leu
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2004A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.916A>C
  hgvsp: ENSP00000311453.4:p.Ile306Leu
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.916A>C
  hgvsp: ENSP00000378056.1:p.Ile306Leu
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*150A>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.700A>C
  hgvsp: ENSP00000453808.1:p.Ile234Leu
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11042A>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile306Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-85641244-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641244
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641244
    reference: chr 15
allele count: 1
allele frequency: 8.445232666159953e-6
allele num: 118410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.780A>G
  hgvsp: ENSP00000340679.5:p.Ile260Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.211A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11040A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-2002A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*297A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.918A>G
  hgvsp: ENSP00000311453.4:p.Ile306Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.702A>G
  hgvsp: ENSP00000453808.1:p.Ile234Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*5A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.918A>G
  hgvsp: ENSP00000378056.1:p.Ile306Met
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*152A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2388A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13850
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile306Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

15-85641266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641266
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641266
    reference: chr 15
allele count: 1
allele frequency: 8.684173961372795e-6
allele num: 115152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.802G>A
  hgvsp: ENSP00000340679.5:p.Gly268Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*319G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*27G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2410G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.724G>A
  hgvsp: ENSP00000453808.1:p.Gly242Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11018G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*174G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.233G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.940G>A
  hgvsp: ENSP00000378056.1:p.Gly314Arg
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-1980G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.940G>A
  hgvsp: ENSP00000311453.4:p.Gly314Arg
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly314Arg
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

15-85641274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641274
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641274
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 113536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.941+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.803+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*175+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2411+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.941+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-1972G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*320+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.234+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.725+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*28+7G>A
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11010G>A
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.941+7G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-85641276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641276
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641276
    reference: chr 15
allele count: 1
allele frequency: 8.842202062001521e-6
allele num: 113094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*320+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000560789
  gene symbol: PDE8A
  hgvsc: ENST00000560789.1:n.2411+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000558543
  gene symbol: PDE8A
  hgvsc: ENST00000558543.1:n.234+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000340679
  ensembl transcript: ENST00000339708
  gene symbol: PDE8A
  hgvsc: ENST00000339708.5:c.803+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000454094
  ensembl transcript: ENST00000559086
  gene symbol: PDE8A
  hgvsc: ENST00000559086.1:c.*80-11008A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.941+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl transcript: ENST00000557819
  gene symbol: PDE8A
  hgvsc: ENST00000557819.2:n.379-1970A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000311453
  ensembl transcript: ENST00000310298
  gene symbol: PDE8A
  hgvsc: ENST00000310298.4:c.941+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*28+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000432309
  ensembl transcript: ENST00000478717
  gene symbol: PDE8A
  hgvsc: ENST00000478717.1:c.*175+9A>G
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000453808
  ensembl transcript: ENST00000557957
  gene symbol: PDE8A
  hgvsc: ENST00000557957.1:c.725+9A>G
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

15-85641290-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85641290
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 85641290
    reference: chr 15
allele count: 12
allele frequency: 1.088178751496246e-4
allele num: 110276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000431976
  ensembl transcript: ENST00000485596
  gene symbol: PDE8A
  hgvsc: ENST00000485596.1:c.*320+23T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000378056
  ensembl transcript: ENST00000394553
  gene symbol: PDE8A
  hgvsc: ENST00000394553.1:c.941+23T>C
  variant of: http://identifiers.org/hgnc/8793
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073417
  ensembl protein: ENSP00000452907
  ensembl transcript: ENST00000559742
  gene symbol: PDE8A
  hgvsc: ENST00000559742.1:c.*28+23T>C
  variant of: http://identifiers.org/hgnc/8793
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1395
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6451
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12155
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3697
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6343
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3841
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5960
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.925345190732506e-5
allele num: 34184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12468
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.256e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.855e0

QD
type: SiteQuality
SIO_000300: 6.92e0

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.171997e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.299e0

GenotypeQuality
all individuals: 1868
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3845
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4362
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6501
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3673
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6019
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5183
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.916982673122922e-5
allele num: 34282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4260
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

DP
type: SiteQuality
SIO_000300: 1.169703e6

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

QD
type: SiteQuality
SIO_000300: 1.165e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.184e0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2641
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9635
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.638522427440633e-4
allele num: 3790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.666666666666667e-2
allele num: 60
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 3.144e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.48e-2

DP
type: SiteQuality
SIO_000300: 8.9124e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

MQ
type: SiteQuality
SIO_000300: 6.102e1

QD
type: SiteQuality
SIO_000300: 9.15e0

GenotypeQuality
all individuals: 459
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1645
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2040
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.947040498442368e-4
allele num: 5136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.641e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -3.339e0

FS
type: SiteQuality
SIO_000300: 2.643e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-2

DP
type: SiteQuality
SIO_000300: 1.09857e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 4.53e0

GenotypeQuality
all individuals: 343
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9699
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.766160367361356e-4
allele num: 5662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2172
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.075e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.16e-1

DP
type: SiteQuality
SIO_000300: 1.18517e5

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9405
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 920
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3693
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 7.780507780507781e-3
allele num: 2442
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.196e0

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.37135e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.083e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

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

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8289
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1263
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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South Asian
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East Asian
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Other
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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FS
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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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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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Latino
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South Asian
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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Other
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European (Finnish)
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South Asian
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DP
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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QD
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InbreedingCoeff
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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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South Asian
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East Asian
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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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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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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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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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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DP
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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MQ
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.312e0

MQRankSum
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SIO_000300: 5.6e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 6600
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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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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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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allele count: 4
allele frequency: 2.452182442373713e-4
allele num: 16312
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.011503945070168e-5
allele num: 66412
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QD
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DP
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
type: SiteQuality
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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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South Asian
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allele frequency: 1.220703125e-4
allele num: 16384
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.633986928104575e-3
allele num: 8568
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Latino
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num of homozygotes: 0

Other
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ReadPosRankSum
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SIO_000300: 7.19e-1

FS
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InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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QD
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele num: 10310
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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allele num: 66484
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South Asian
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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FS
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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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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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African
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East Asian
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Other
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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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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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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African
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Latino
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South Asian
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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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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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5340
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 3
allele frequency: 1.825928180158247e-4
allele num: 16430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

DP
type: SiteQuality
SIO_000300: 1.619173e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.31e-1

FS
type: SiteQuality
SIO_000300: 3.411e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.23e-1

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

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

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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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503171692270691e-5
allele num: 66526
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.619969e6

VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 1.273e0

QD
type: SiteQuality
SIO_000300: 1.08e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.509e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
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: 8552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 6.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

FS
type: SiteQuality
SIO_000300: 3.743e0

DP
type: SiteQuality
SIO_000300: 1.620895e6

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.785e0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 773
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GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
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: 8556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.258e0

QD
type: SiteQuality
SIO_000300: 1.289e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.467e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

DP
type: SiteQuality
SIO_000300: 1.621963e6

FS
type: SiteQuality
SIO_000300: 6.201e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: -2.282e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1422
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 620
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 171
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variant carriers: 0

GenotypeQuality
all individuals: 234
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

FS
type: SiteQuality
SIO_000300: 4.072e0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.623003e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.89e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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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: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505298651252408e-5
allele num: 66432
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.848e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 1.778e0

DP
type: SiteQuality
SIO_000300: 1.619663e6

GenotypeQuality
all individuals: 90
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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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bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.68429207824908e-5
allele num: 10326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.848e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 1.778e0

DP
type: SiteQuality
SIO_000300: 1.619663e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.238e0

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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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
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: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.011141222523336e-5
allele num: 66420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.541326067211626e-4
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.619247e6

FS
type: SiteQuality
SIO_000300: 5.22e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
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allele frequency: 0.0e0
allele num: 15764
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

African
type: Population
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allele frequency: 1.937233630375823e-4
allele num: 10324
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.486e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.614559e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.626905235255136e-5
allele num: 15090
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

MQ
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SIO_000300: 6.0e1

DP
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

BaseQRankSum
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SIO_000300: 2.45e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11528
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.791632708503124e-5
allele num: 14724
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.61e-1

FS
type: SiteQuality
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QD
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

South 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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.528771479239283e-5
allele num: 65412
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.086e0

DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: 3.82e-1

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65362
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South Asian
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
allele num: 8522
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European (Finnish)
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allele frequency: 0.0e0
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Other
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 9.852216748768474e-5
allele num: 10150
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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South Asian
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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FS
type: SiteQuality
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MQ
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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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variant carriers: 1

European (Non-Finnish)
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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allele num: 8498
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South Asian
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FS
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SIO_000300: 3.3e0

QD
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SIO_000300: 9.94e0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.563e0

DP
type: SiteQuality
SIO_000300: 1.517222e6

MQ
type: SiteQuality
SIO_000300: 6.055e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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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bin: 2.25e1
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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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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549714852467146e-5
allele num: 64528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.766e0

MQRankSum
type: SiteQuality
SIO_000300: 9.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 1.536e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 1.489049e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

VQSLOD
type: SiteQuality
SIO_000300: -1.192e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.772421127259837e-4
allele num: 11284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64394
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.483173e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.794687724335966e-4
allele num: 11144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64310
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

FS
type: SiteQuality
SIO_000300: 1.794e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

DP
type: SiteQuality
SIO_000300: 1.478568e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

GenotypeQuality
all individuals: 66
bin: 2.5e0
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: 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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variant carriers: 0

GenotypeQuality
all individuals: 2488
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GenotypeQuality
all individuals: 477
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.078515962036238e-4
allele num: 9272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14732
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.283611e6

QD
type: SiteQuality
SIO_000300: 8.08e0

VQSLOD
type: SiteQuality
SIO_000300: -6.673e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeQuality
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bin: 3.25e1
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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1101
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60948
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.921229586935639e-4
allele num: 10410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14740
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.35e-1

FS
type: SiteQuality
SIO_000300: 1.877e0

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.322522e6

QD
type: SiteQuality
SIO_000300: 1.249e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5350
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.63510906177442e-5
allele num: 61158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.227888960619754e-4
allele num: 9294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10432
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 1.32998e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 5.396e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

QD
type: SiteQuality
SIO_000300: 1.395e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1188
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.061120543293718e-4
allele num: 9424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.624947864865732e-5
allele num: 62338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 7.754e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
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SIO_000300: -1.754e0

QD
type: SiteQuality
SIO_000300: 1.197e1

MQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.421133e6

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1604
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GenotypeQuality
all individuals: 4222
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.596169193934557e-5
allele num: 62650
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 7.382408774520143e-4
allele num: 9482
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East Asian
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allele frequency: 1.242236024844721e-4
allele num: 8050
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.572524845892565e-5
allele num: 63592
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6484
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8256
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.688525614978276e-5
allele num: 63986
num of homozygotes: 0

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

Latino
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VQSLOD
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FS
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 2.9e-3

ClippingRankSum
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SIO_000300: -1.55e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64176
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15518
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 9.105809506465124e-5
allele num: 10982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 5.85e-1

ClippingRankSum
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FS
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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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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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 64252
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 64854
num of homozygotes: 0

European (Finnish)
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East Asian
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African
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Latino
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South Asian
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QD
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 65614
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South Asian
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65792
num of homozygotes: 0

Latino
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European (Finnish)
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Other
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African
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.524e0

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 9.21e-1

QD
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SIO_000300: 1.584e1

DP
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SIO_000300: 1.537587e6

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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bin: 9.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65956
num of homozygotes: 0

African
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South Asian
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Other
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East Asian
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MQ
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VQSLOD
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FS
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MQRankSum
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DP
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.277e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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African
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allele frequency: 0.0e0
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South Asian
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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SIO_000300: -2.144e0

QD
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SIO_000300: 8.800000000000001e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66034
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African
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allele count: 1
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allele num: 10080
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South Asian
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allele frequency: 0.0e0
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Other
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QD
type: SiteQuality
SIO_000300: 1.385e1

BaseQRankSum
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SIO_000300: 4.9e0

FS
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SIO_000300: 0.0e0

MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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VQSLOD
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SIO_000300: 3.51e-1

ClippingRankSum
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SIO_000300: -8.799999999999999e-2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 2
allele frequency: 2.341372044017794e-4
allele num: 8542
num of homozygotes: 0

South Asian
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allele frequency: 6.185056902523504e-5
allele num: 16168
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African
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Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 6.05858653176214e-5
allele num: 66022
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VQSLOD
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.924573243350536e-5
allele num: 10076
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66028
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South Asian
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FS
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65934
num of homozygotes: 0

South Asian
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allele frequency: 1.239464551313832e-4
allele num: 16136
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.858965272856131e-5
allele num: 11288
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8532
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65872
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African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.52031135976648e-5
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African
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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DP
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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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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65648
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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African
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East Asian
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FS
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.525553012967201e-5
allele num: 65550
num of homozygotes: 0

South Asian
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Latino
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European (Finnish)
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num of homozygotes: 0

East Asian
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allele num: 8492
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Other
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African
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ClippingRankSum
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SIO_000300: 2.13e-1

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

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

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

East Asian
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African
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Latino
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European (Finnish)
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Other
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South Asian
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9018
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2968
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 800
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3954
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.510416666666667e-5
allele num: 15360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.118e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.787e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.819e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

DP
type: SiteQuality
SIO_000300: 1.412771e6

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0