22-32017553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017553
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017553
    reference: chr 22
allele count: 1
allele frequency: 9.188811702870585e-6
allele num: 108828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.635C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.647C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+82C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+85C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14153
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/22-32017556-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017556
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017555
    reference: chr 22
allele count: 28
allele frequency: 2.584790355039418e-4
allele num: 108326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+81delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.643delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.631delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+78delG
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+78delG
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8238
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12936
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13510
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AC
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

22-32017557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017557
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017557
    reference: chr 22
allele count: 7
allele frequency: 6.486286137879912e-5
allele num: 107920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.631G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+81G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.643G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+78G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+78G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13666
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12855
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13843
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

22-32017558-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017558
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017558
    reference: chr 22
allele count: 2
allele frequency: 1.846722068328717e-5
allele num: 108300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+80C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.630C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.642C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+77C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+77C>G
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13918
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

22-32017561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017561
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017561
    reference: chr 22
allele count: 1
allele frequency: 9.254289363119806e-6
allele num: 108058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.627C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+77C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.639C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+74C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14800
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

22-32017564-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017564
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017564
    reference: chr 22
allele count: 1
allele frequency: 9.255831173639393e-6
allele num: 108040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.624C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.636C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+74C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+71C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+71C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12523
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/22-32017565-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017565
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017565
    reference: chr 22
allele count: 1
allele frequency: 9.2397531137968e-6
allele num: 108228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.635T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+73T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.623T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+70T>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+70T>G
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12469
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/22-32017567-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017567
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017566
    reference: chr 22
allele count: 1
allele frequency: 9.209799226376865e-6
allele num: 108580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+70delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.632delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+67delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.620delT
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+67delT
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11796
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: CA
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

22-32017587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017587
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017587
    reference: chr 22
allele count: 600
allele frequency: 5.267038870746866e-3
allele num: 113916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.601C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+51C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.613C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+48C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+48C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13115
  bin: 1.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 1.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14174
  bin: 2.25e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 16
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

22-32017592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017592
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017592
    reference: chr 22
allele count: 1
allele frequency: 8.776395007986519e-6
allele num: 113942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.608C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+46C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.596C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+43C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+43C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9081
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

22-32017595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017595
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017595
    reference: chr 22
allele count: 1
allele frequency: 8.756260726419389e-6
allele num: 114204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.605T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.593T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+43T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+40T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+40T>C
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9483
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/22-32017608-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017608
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017608
    reference: chr 22
allele count: 3
allele frequency: 2.614925997594268e-5
allele num: 114726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.592G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+30G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+27G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.580G>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13013
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

22-32017614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017614
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017614
    reference: chr 22
allele count: 23
allele frequency: 1.995730871353453e-4
allele num: 115246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.574C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.586C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+24C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+21C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+21C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13891
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23886
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

22-32017615-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017615
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017615
    reference: chr 22
allele count: 2
allele frequency: 1.733432716809097e-5
allele num: 115378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.573T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.585T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+20T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+23T>C
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

22-32017621-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017621
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017621
    reference: chr 22
allele count: 1
allele frequency: 8.633192900062159e-6
allele num: 115832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.579C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.567C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+14C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+17C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+14C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25420
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/22-32017629-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017629
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017629
    reference: chr 22
allele count: 1
allele frequency: 8.566484486096596e-6
allele num: 116734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.609+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.456+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*307+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.456+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.558+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.530+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.270+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.462+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.456+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.456+6G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.571G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.559G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+9G>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25865
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.456+6G>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

22-32017637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017637
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017637
    reference: chr 22
allele count: 3
allele frequency: 2.549632852869187e-5
allele num: 117664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.556G>A
  hgvsp: ENSP00000391739.2:p.Val186Met
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.454G>A
  hgvsp: ENSP00000371586.2:p.Val152Met
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.454G>A
  hgvsp: ENSP00000380637.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.454G>A
  hgvsp: ENSP00000266095.5:p.Val152Met
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.454G>A
  hgvsp: ENSP00000412169.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*305G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.528G>A
  hgvsp: ENSP00000414395.1:p.Val177Met
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.555+1G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.268G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.460G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.551G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.607G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.563G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.555+1G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

22-32017642-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017642
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017642
    reference: chr 22
allele count: 1
allele frequency: 8.448657508321927e-6
allele num: 118362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*300A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.558A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.551A>G
  hgvsp: ENSP00000338695.4:p.His184Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.602A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.449A>G
  hgvsp: ENSP00000380637.1:p.His150Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.455A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.449A>G
  hgvsp: ENSP00000371586.2:p.His150Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.523A>G
  hgvsp: ENSP00000414395.1:p.His175Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.546A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.449A>G
  hgvsp: ENSP00000412169.1:p.His150Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.449A>G
  hgvsp: ENSP00000266095.5:p.His150Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.551A>G
  hgvsp: ENSP00000391739.2:p.His184Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.263A>G
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His150Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-32017642-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017642
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017642
    reference: chr 22
allele count: 3
allele frequency: 2.534597252496578e-5
allele num: 118362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.449A>C
  hgvsp: ENSP00000412169.1:p.His150Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.449A>C
  hgvsp: ENSP00000380637.1:p.His150Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.523A>C
  hgvsp: ENSP00000414395.1:p.His175Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.551A>C
  hgvsp: ENSP00000391739.2:p.His184Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.551A>C
  hgvsp: ENSP00000338695.4:p.His184Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.449A>C
  hgvsp: ENSP00000266095.5:p.His150Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.558A>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.449A>C
  hgvsp: ENSP00000371586.2:p.His150Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.602A>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*300A>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.263A>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.546A>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.455A>C
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His150Pro
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/22-32017648-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017648
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017648
    reference: chr 22
allele count: 1
allele frequency: 8.414958430105355e-6
allele num: 118836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.443G>T
  hgvsp: ENSP00000380637.1:p.Gly148Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.552G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.443G>T
  hgvsp: ENSP00000266095.5:p.Gly148Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.545G>T
  hgvsp: ENSP00000338695.4:p.Gly182Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.517G>T
  hgvsp: ENSP00000414395.1:p.Gly173Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.443G>T
  hgvsp: ENSP00000412169.1:p.Gly148Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*294G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.443G>T
  hgvsp: ENSP00000371586.2:p.Gly148Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.540G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.257G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.449G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.596G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.545G>T
  hgvsp: ENSP00000391739.2:p.Gly182Val
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly148Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

22-32017655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017655
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017655
    reference: chr 22
allele count: 11
allele frequency: 9.234075417212316e-5
allele num: 119124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.442G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.436G>A
  hgvsp: ENSP00000266095.5:p.Val146Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.250G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.589G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.545G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.510G>A
  hgvsp: ENSP00000414395.1:p.Val171Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.436G>A
  hgvsp: ENSP00000380637.1:p.Val146Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.533G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*287G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.538G>A
  hgvsp: ENSP00000391739.2:p.Val180Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.538G>A
  hgvsp: ENSP00000338695.4:p.Val180Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.436G>A
  hgvsp: ENSP00000412169.1:p.Val146Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.436G>A
  hgvsp: ENSP00000371586.2:p.Val146Ile
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val146Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

22-32017659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017659
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017659
    reference: chr 22
allele count: 45
allele frequency: 3.773584905660377e-4
allele num: 119250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.541G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.534G>A
  hgvsp: ENST00000439502.2:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.246G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.534G>A
  hgvsp: ENST00000336566.4:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.438G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.506G>A
  hgvsp: ENST00000435900.1:c.506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.432G>A
  hgvsp: ENST00000266095.5:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.432G>A
  hgvsp: ENST00000397500.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.432G>A
  hgvsp: ENST00000382151.2:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.529G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*283G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.585G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.432G>A
  hgvsp: ENST00000422020.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26425
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17950
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8146
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Arg144Arg
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

22-32017660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017660
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017660
    reference: chr 22
allele count: 4
allele frequency: 3.361344537815126e-5
allele num: 119000
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.431G>A
  hgvsp: ENSP00000371586.2:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.431G>A
  hgvsp: ENSP00000266095.5:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.533G>A
  hgvsp: ENSP00000391739.2:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.533G>A
  hgvsp: ENSP00000338695.4:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.431G>A
  hgvsp: ENSP00000412169.1:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.505G>A
  hgvsp: ENSP00000414395.1:p.Arg169Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.431G>A
  hgvsp: ENSP00000380637.1:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.584G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.540G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.437G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.528G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.245G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*282G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg144Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

22-32017661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017661
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017661
    reference: chr 22
allele count: 2
allele frequency: 1.676474039799494e-5
allele num: 119298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.532C>T
  hgvsp: ENSP00000391739.2:p.Arg178Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.532C>T
  hgvsp: ENSP00000338695.4:p.Arg178Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.436C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*281C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.430C>T
  hgvsp: ENSP00000380637.1:p.Arg144Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.504C>T
  hgvsp: ENSP00000414395.1:p.Arg169Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.244C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.430C>T
  hgvsp: ENSP00000266095.5:p.Arg144Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.539C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.583C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.430C>T
  hgvsp: ENSP00000371586.2:p.Arg144Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.430C>T
  hgvsp: ENSP00000412169.1:p.Arg144Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.527C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8255
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg144Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

22-32017662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017662
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017662
    reference: chr 22
allele count: 15
allele frequency: 1.257018352467946e-4
allele num: 119330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.531C>T
  hgvsp: ENST00000336566.4:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.243C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.429C>T
  hgvsp: ENST00000422020.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*280C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.503C>T
  hgvsp: ENST00000435900.1:c.503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.429C>T
  hgvsp: ENST00000382151.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.538C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.429C>T
  hgvsp: ENST00000397500.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.582C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.531C>T
  hgvsp: ENST00000439502.2:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.435C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.526C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.429C>T
  hgvsp: ENST00000266095.5:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26005
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala143Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

22-32017662-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017662
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017662
    reference: chr 22
allele count: 1
allele frequency: 8.380122349786308e-6
allele num: 119330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.429C>G
  hgvsp: ENST00000397500.1:c.429C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.243C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*280C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.531C>G
  hgvsp: ENST00000336566.4:c.531C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.429C>G
  hgvsp: ENST00000382151.2:c.429C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.429C>G
  hgvsp: ENST00000266095.5:c.429C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.526C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.435C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.538C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.429C>G
  hgvsp: ENST00000422020.1:c.429C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.531C>G
  hgvsp: ENST00000439502.2:c.531C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.582C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.503C>G
  hgvsp: ENST00000435900.1:c.503C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala143Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum

22-32017668-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017668
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017668
    reference: chr 22
allele count: 11
allele frequency: 9.223854564969477e-5
allele num: 119256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.497G>A
  hgvsp: ENST00000435900.1:c.497G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.520G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.429G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*274G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.423G>A
  hgvsp: ENST00000422020.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.423G>A
  hgvsp: ENST00000397500.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.525G>A
  hgvsp: ENST00000439502.2:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.525G>A
  hgvsp: ENST00000336566.4:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.237G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.532G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.423G>A
  hgvsp: ENST00000266095.5:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.576G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.423G>A
  hgvsp: ENST00000382151.2:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18076
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25604
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro141Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

22-32017669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017669
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017669
    reference: chr 22
allele count: 1
allele frequency: 8.361623492817366e-6
allele num: 119594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.422C>T
  hgvsp: ENSP00000380637.1:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.496C>T
  hgvsp: ENSP00000414395.1:p.Pro166Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.524C>T
  hgvsp: ENSP00000391739.2:p.Pro175Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.519C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.428C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.531C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.236C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.422C>T
  hgvsp: ENSP00000412169.1:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.524C>T
  hgvsp: ENSP00000338695.4:p.Pro175Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.422C>T
  hgvsp: ENSP00000266095.5:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.575C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.422C>T
  hgvsp: ENSP00000371586.2:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro141Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-32017670-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017670
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017670
    reference: chr 22
allele count: 5
allele frequency: 4.178994701034719e-5
allele num: 119646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.421C>A
  hgvsp: ENSP00000412169.1:p.Pro141Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*272C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.518C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.235C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.523C>A
  hgvsp: ENSP00000391739.2:p.Pro175Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.495C>A
  hgvsp: ENSP00000414395.1:p.Pro166Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.523C>A
  hgvsp: ENSP00000338695.4:p.Pro175Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.421C>A
  hgvsp: ENSP00000266095.5:p.Pro141Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.421C>A
  hgvsp: ENSP00000380637.1:p.Pro141Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.530C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.427C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.574C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.421C>A
  hgvsp: ENSP00000371586.2:p.Pro141Thr
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro141Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-32017683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017683
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017683
    reference: chr 22
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.408G>A
  hgvsp: ENST00000382151.2:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*259G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.408G>A
  hgvsp: ENST00000397500.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.561G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.510G>A
  hgvsp: ENST00000439502.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.408G>A
  hgvsp: ENST00000266095.5:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.505G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.482G>A
  hgvsp: ENST00000435900.1:c.482G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.510G>A
  hgvsp: ENST00000336566.4:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.517G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.414G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.408G>A
  hgvsp: ENST00000422020.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.222G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26406
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg136Arg
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-32017684-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017684
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017684
    reference: chr 22
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.509G>A
  hgvsp: ENSP00000338695.4:p.Arg170Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.407G>A
  hgvsp: ENSP00000412169.1:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.407G>A
  hgvsp: ENSP00000380637.1:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*258G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.407G>A
  hgvsp: ENSP00000371586.2:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.481G>A
  hgvsp: ENSP00000414395.1:p.Arg161Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.509G>A
  hgvsp: ENSP00000391739.2:p.Arg170Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.407G>A
  hgvsp: ENSP00000266095.5:p.Arg136Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.413G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.504G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.516G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.560G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.221G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg136Gln
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-32017684-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017684
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017684
    reference: chr 22
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*258G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.481G>T
  hgvsp: ENSP00000414395.1:p.Arg161Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.504G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.560G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.407G>T
  hgvsp: ENSP00000371586.2:p.Arg136Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.516G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.407G>T
  hgvsp: ENSP00000412169.1:p.Arg136Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.407G>T
  hgvsp: ENSP00000380637.1:p.Arg136Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.221G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.509G>T
  hgvsp: ENSP00000391739.2:p.Arg170Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.509G>T
  hgvsp: ENSP00000338695.4:p.Arg170Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.407G>T
  hgvsp: ENSP00000266095.5:p.Arg136Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.413G>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg136Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

22-32017689-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017689
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017689
    reference: chr 22
allele count: 7
allele frequency: 5.801040872476547e-5
allele num: 120668
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.402C>A
  hgvsp: ENSP00000371586.2:p.Phe134Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.555C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.504C>A
  hgvsp: ENSP00000338695.4:p.Phe168Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.402C>A
  hgvsp: ENSP00000380637.1:p.Phe134Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.511C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.402C>A
  hgvsp: ENSP00000266095.5:p.Phe134Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.476C>A
  hgvsp: ENSP00000414395.1:p.Phe159Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*253C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.499C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.504C>A
  hgvsp: ENSP00000391739.2:p.Phe168Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.408C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.402C>A
  hgvsp: ENSP00000412169.1:p.Phe134Leu
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.216C>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe134Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

22-32017700-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017700
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017700
    reference: chr 22
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.500C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.397C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.493C>A
  hgvsp: ENSP00000338695.4:p.Leu165Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.493C>A
  hgvsp: ENSP00000391739.2:p.Leu165Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.391C>A
  hgvsp: ENSP00000380637.1:p.Leu131Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*242C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.465C>A
  hgvsp: ENSP00000414395.1:p.Leu156Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.391C>A
  hgvsp: ENSP00000266095.5:p.Leu131Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.205C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.544C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.391C>A
  hgvsp: ENSP00000412169.1:p.Leu131Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.488C>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.391C>A
  hgvsp: ENSP00000371586.2:p.Leu131Ile
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu131Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

22-32017703-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017703
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017703
    reference: chr 22
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.388A>G
  hgvsp: ENSP00000371586.2:p.Asn130Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.388A>G
  hgvsp: ENSP00000266095.5:p.Asn130Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.490A>G
  hgvsp: ENSP00000338695.4:p.Asn164Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*239A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.541A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.388A>G
  hgvsp: ENSP00000412169.1:p.Asn130Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.394A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.388A>G
  hgvsp: ENSP00000380637.1:p.Asn130Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.485A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.462A>G
  hgvsp: ENSP00000414395.1:p.Asn155Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.497A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.490A>G
  hgvsp: ENSP00000391739.2:p.Asn164Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.202A>G
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn130Asp
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

22-32017705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017705
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017705
    reference: chr 22
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.460G>A
  hgvsp: ENSP00000414395.1:p.Arg154His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.539G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.488G>A
  hgvsp: ENSP00000338695.4:p.Arg163His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.386G>A
  hgvsp: ENSP00000412169.1:p.Arg129His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.392G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.495G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.488G>A
  hgvsp: ENSP00000391739.2:p.Arg163His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.386G>A
  hgvsp: ENSP00000371586.2:p.Arg129His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*237G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.386G>A
  hgvsp: ENSP00000266095.5:p.Arg129His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.483G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.386G>A
  hgvsp: ENSP00000380637.1:p.Arg129His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.200G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg129His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

22-32017706-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017706
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017706
    reference: chr 22
allele count: 6
allele frequency: 4.953355898621316e-5
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.385C>T
  hgvsp: ENSP00000371586.2:p.Arg129Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.487C>T
  hgvsp: ENSP00000338695.4:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.385C>T
  hgvsp: ENSP00000266095.5:p.Arg129Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.494C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*236C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.391C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.538C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.385C>T
  hgvsp: ENSP00000380637.1:p.Arg129Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.487C>T
  hgvsp: ENSP00000391739.2:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.385C>T
  hgvsp: ENSP00000412169.1:p.Arg129Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.459C>T
  hgvsp: ENSP00000414395.1:p.Arg154Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.482C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.199C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg129Cys
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

22-32017707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017707
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017707
    reference: chr 22
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*235C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.384C>T
  hgvsp: ENST00000422020.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.198C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.384C>T
  hgvsp: ENST00000397500.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.486C>T
  hgvsp: ENST00000439502.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.537C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.486C>T
  hgvsp: ENST00000336566.4:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.481C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.458C>T
  hgvsp: ENST00000435900.1:c.458C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.384C>T
  hgvsp: ENST00000382151.2:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.390C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.384C>T
  hgvsp: ENST00000266095.5:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.493C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr128Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS

22-32017716-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017716
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017716
    reference: chr 22
allele count: 4
allele frequency: 3.3003300330033e-5
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.375G>A
  hgvsp: ENST00000266095.5:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.375G>A
  hgvsp: ENST00000382151.2:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.472G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.189G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.375G>A
  hgvsp: ENST00000422020.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.381G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.528G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.484G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.375G>A
  hgvsp: ENST00000397500.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.449G>A
  hgvsp: ENST00000435900.1:c.449G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.477G>A
  hgvsp: ENST00000439502.2:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.477G>A
  hgvsp: ENST00000336566.4:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu125Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-32017717-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017717
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017717
    reference: chr 22
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.380T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.527T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.471T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.476T>C
  hgvsp: ENSP00000338695.4:p.Leu159Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.374T>C
  hgvsp: ENSP00000380637.1:p.Leu125Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.374T>C
  hgvsp: ENSP00000266095.5:p.Leu125Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.476T>C
  hgvsp: ENSP00000391739.2:p.Leu159Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*225T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.188T>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.448T>C
  hgvsp: ENSP00000414395.1:p.Leu150Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.374T>C
  hgvsp: ENSP00000371586.2:p.Leu125Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.374T>C
  hgvsp: ENSP00000412169.1:p.Leu125Pro
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.483T>C
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu125Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

22-32017730-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017730
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017730
    reference: chr 22
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.435G>A
  hgvsp: ENSP00000414395.1:p.Ala146Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.361G>A
  hgvsp: ENSP00000412169.1:p.Ala121Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.463G>A
  hgvsp: ENSP00000391739.2:p.Ala155Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.367G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*212G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.361G>A
  hgvsp: ENSP00000371586.2:p.Ala121Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.470G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.361G>A
  hgvsp: ENSP00000266095.5:p.Ala121Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.463G>A
  hgvsp: ENSP00000338695.4:p.Ala155Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.361G>A
  hgvsp: ENSP00000380637.1:p.Ala121Thr
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.514G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.458G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.175G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala121Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

22-32017731-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017731
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017731
    reference: chr 22
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.513C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.174C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.360C>T
  hgvsp: ENST00000266095.5:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.360C>T
  hgvsp: ENST00000382151.2:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.469C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*211C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.462C>T
  hgvsp: ENST00000439502.2:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.434C>T
  hgvsp: ENST00000435900.1:c.434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.360C>T
  hgvsp: ENST00000397500.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.360C>T
  hgvsp: ENST00000422020.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.462C>T
  hgvsp: ENST00000336566.4:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.457C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.366C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala120Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/22-32017750-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017750
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017750
    reference: chr 22
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.450G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.347G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.438G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.443G>T
  hgvsp: ENSP00000391739.2:p.Gly148Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.341G>T
  hgvsp: ENSP00000266095.5:p.Gly114Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.341G>T
  hgvsp: ENSP00000380637.1:p.Gly114Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.341G>T
  hgvsp: ENSP00000412169.1:p.Gly114Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*192G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.415G>T
  hgvsp: ENSP00000414395.1:p.Gly139Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.155G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.341G>T
  hgvsp: ENSP00000371586.2:p.Gly114Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.443G>T
  hgvsp: ENSP00000338695.4:p.Gly148Val
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.494G>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly114Val
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

22-32017755-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017755
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017755
    reference: chr 22
allele count: 5
allele frequency: 4.123167252156417e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.410G>A
  hgvsp: ENST00000435900.1:c.410G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.438G>A
  hgvsp: ENST00000439502.2:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.336G>A
  hgvsp: ENST00000397500.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.342G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.336G>A
  hgvsp: ENST00000422020.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.489G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.438G>A
  hgvsp: ENST00000336566.4:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*187G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.445G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.336G>A
  hgvsp: ENST00000382151.2:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.336G>A
  hgvsp: ENST00000266095.5:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.433G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.150G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr112Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

22-32017757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017757
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017757
    reference: chr 22
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.436A>G
  hgvsp: ENSP00000391739.2:p.Thr146Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.334A>G
  hgvsp: ENSP00000412169.1:p.Thr112Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.408A>G
  hgvsp: ENSP00000414395.1:p.Thr137Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*185A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.334A>G
  hgvsp: ENSP00000380637.1:p.Thr112Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.334A>G
  hgvsp: ENSP00000371586.2:p.Thr112Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.443A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.436A>G
  hgvsp: ENSP00000338695.4:p.Thr146Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.431A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.334A>G
  hgvsp: ENSP00000266095.5:p.Thr112Ala
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.340A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.148A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.487A>G
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr112Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

22-32017760-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017760
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017761
    reference: chr 22
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.144_145insA
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.330_331insA
  hgvsp: ENSP00000380637.1:p.Trp111MetfsTer44
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.330_331insA
  hgvsp: ENSP00000371586.2:p.Trp111MetfsTer44
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*181_*182insA
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.483_484insA
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.330_331insA
  hgvsp: ENSP00000266095.5:p.Trp111MetfsTer44
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.404_405insA
  hgvsp: ENSP00000414395.1:p.Trp136MetfsTer44
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.330_331insA
  hgvsp: ENSP00000412169.1:p.Trp111MetfsTer44
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.432_433insA
  hgvsp: ENSP00000391739.2:p.Trp145MetfsTer44
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.432_433insA
  hgvsp: ENSP00000338695.4:p.Trp145MetfsTer43
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.427_428insA
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.336_337insA
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.439_440insA
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp111MetfsTer44
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

22-32017761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017761
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017761
    reference: chr 22
allele count: 17
allele frequency: 1.402246894435554e-4
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.432C>T
  hgvsp: ENST00000439502.2:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.330C>T
  hgvsp: ENST00000266095.5:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.144C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.432C>T
  hgvsp: ENST00000336566.4:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.330C>T
  hgvsp: ENST00000422020.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.330C>T
  hgvsp: ENST00000397500.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.336C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.404C>T
  hgvsp: ENST00000435900.1:c.404C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.439C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.330C>T
  hgvsp: ENST00000382151.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.483C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.427C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 26958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile110Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

22-32017764-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017764
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017764
    reference: chr 22
allele count: 2
allele frequency: 1.650056101907465e-5
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.429C>T
  hgvsp: ENST00000439502.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.327C>T
  hgvsp: ENST00000266095.5:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.436C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.401C>T
  hgvsp: ENST00000435900.1:c.401C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.327C>T
  hgvsp: ENST00000397500.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.327C>T
  hgvsp: ENST00000382151.2:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.141C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.480C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*178C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.327C>T
  hgvsp: ENST00000422020.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.429C>T
  hgvsp: ENST00000336566.4:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.424C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.333C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr109Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

22-32017770-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017770
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017770
    reference: chr 22
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.327C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.321C>T
  hgvsp: ENST00000397500.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.321C>T
  hgvsp: ENST00000382151.2:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.321C>T
  hgvsp: ENST00000422020.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.321C>T
  hgvsp: ENST00000266095.5:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.430C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.395C>T
  hgvsp: ENST00000435900.1:c.395C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.423C>T
  hgvsp: ENST00000336566.4:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.418C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.135C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.423C>T
  hgvsp: ENST00000439502.2:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.474C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser107Ser
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: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

22-32017778-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017778
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017778
    reference: chr 22
allele count: 13
allele frequency: 1.076515402451143e-4
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.313G>A
  hgvsp: ENSP00000266095.5:p.Val105Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.415G>A
  hgvsp: ENSP00000338695.4:p.Val139Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.313G>A
  hgvsp: ENSP00000380637.1:p.Val105Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.127G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.410G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.387G>A
  hgvsp: ENSP00000414395.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*164G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.422G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.415G>A
  hgvsp: ENSP00000391739.2:p.Val139Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.313G>A
  hgvsp: ENSP00000412169.1:p.Val105Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.313G>A
  hgvsp: ENSP00000371586.2:p.Val105Ile
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.466G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.319G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val105Ile
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

22-32017779-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017779
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017779
    reference: chr 22
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.318C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.386C>G
  hgvsp: ENST00000435900.1:c.386C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.312C>G
  hgvsp: ENST00000397500.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.126C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.312C>G
  hgvsp: ENST00000266095.5:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.414C>G
  hgvsp: ENST00000439502.2:c.414C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.409C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.414C>G
  hgvsp: ENST00000336566.4:c.414C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.421C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.465C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.312C>G
  hgvsp: ENST00000422020.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*163C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.312C>G
  hgvsp: ENST00000382151.2:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro104Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

22-32017779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017779
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017779
    reference: chr 22
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.318C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.312C>T
  hgvsp: ENST00000397500.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.414C>T
  hgvsp: ENST00000439502.2:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*163C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.312C>T
  hgvsp: ENST00000382151.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.465C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.312C>T
  hgvsp: ENST00000422020.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.421C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.409C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.414C>T
  hgvsp: ENST00000336566.4:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.386C>T
  hgvsp: ENST00000435900.1:c.386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.126C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.312C>T
  hgvsp: ENST00000266095.5:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro104Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

22-32017783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017783
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017783
    reference: chr 22
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.417G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.308G>A
  hgvsp: ENSP00000380637.1:p.Arg103Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.308G>A
  hgvsp: ENSP00000412169.1:p.Arg103Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.122G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*159G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.405G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.410G>A
  hgvsp: ENSP00000338695.4:p.Arg137Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.308G>A
  hgvsp: ENSP00000266095.5:p.Arg103Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.461G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.410G>A
  hgvsp: ENSP00000391739.2:p.Arg137Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.308G>A
  hgvsp: ENSP00000371586.2:p.Arg103Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.382G>A
  hgvsp: ENSP00000414395.1:p.Arg128Lys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.314G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg103Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

22-32017786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017786
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017786
    reference: chr 22
allele count: 2
allele frequency: 1.659117681217129e-5
allele num: 120546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.379G>A
  hgvsp: ENSP00000414395.1:p.Arg127His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.119G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.402G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.305G>A
  hgvsp: ENSP00000266095.5:p.Arg102His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.305G>A
  hgvsp: ENSP00000412169.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.305G>A
  hgvsp: ENSP00000371586.2:p.Arg102His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.305G>A
  hgvsp: ENSP00000380637.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.407G>A
  hgvsp: ENSP00000338695.4:p.Arg136His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.414G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.407G>A
  hgvsp: ENSP00000391739.2:p.Arg136His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.311G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.458G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*156G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg102His
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

22-32017787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017787
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017787
    reference: chr 22
allele count: 1
allele frequency: 8.658908284843448e-6
allele num: 115488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.406C>T
  hgvsp: ENSP00000391739.2:p.Arg136Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.118C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.406C>T
  hgvsp: ENSP00000338695.4:p.Arg136Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.401C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.378C>T
  hgvsp: ENSP00000414395.1:p.Arg127Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*155C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.413C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.304C>T
  hgvsp: ENSP00000371586.2:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.304C>T
  hgvsp: ENSP00000266095.5:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.457C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.304C>T
  hgvsp: ENSP00000412169.1:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.304C>T
  hgvsp: ENSP00000380637.1:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.310C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 8772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg102Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

22-32017787-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017787
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017787
    reference: chr 22
allele count: 59
allele frequency: 5.108755888057634e-4
allele num: 115488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*155C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.413C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.406C>G
  hgvsp: ENSP00000391739.2:p.Arg136Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.304C>G
  hgvsp: ENSP00000380637.1:p.Arg102Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.304C>G
  hgvsp: ENSP00000266095.5:p.Arg102Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.401C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.304C>G
  hgvsp: ENSP00000412169.1:p.Arg102Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.406C>G
  hgvsp: ENSP00000338695.4:p.Arg136Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.304C>G
  hgvsp: ENSP00000371586.2:p.Arg102Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.378C>G
  hgvsp: ENSP00000414395.1:p.Arg127Gly
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.457C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.310C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.118C>G
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25417
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8772
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18993
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg102Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

22-32017799-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017799
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017799
    reference: chr 22
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.292C>T
  hgvsp: ENSP00000412169.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.292C>T
  hgvsp: ENSP00000371586.2:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.292C>T
  hgvsp: ENSP00000380637.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.366C>T
  hgvsp: ENSP00000414395.1:p.Pro123Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.394C>T
  hgvsp: ENSP00000338695.4:p.Pro132Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.292C>T
  hgvsp: ENSP00000266095.5:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.394C>T
  hgvsp: ENSP00000391739.2:p.Pro132Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.401C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.298C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.389C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.106C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.445C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro98Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/22-32017803-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017803
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017803
    reference: chr 22
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.288G>T
  hgvsp: ENSP00000412169.1:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.390G>T
  hgvsp: ENSP00000338695.4:p.Glu130Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.288G>T
  hgvsp: ENSP00000266095.5:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.102G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*139G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.390G>T
  hgvsp: ENSP00000391739.2:p.Glu130Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.294G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.397G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.288G>T
  hgvsp: ENSP00000380637.1:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.385G>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.362G>T
  hgvsp: ENSP00000414395.1:p.Glu121Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.288G>T
  hgvsp: ENSP00000371586.2:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.441G>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu96Asp
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

22-32017805-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017805
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017805
    reference: chr 22
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.388G>C
  hgvsp: ENSP00000391739.2:p.Glu130Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.286G>C
  hgvsp: ENSP00000371586.2:p.Glu96Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.439G>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.100G>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.286G>C
  hgvsp: ENSP00000266095.5:p.Glu96Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.388G>C
  hgvsp: ENSP00000338695.4:p.Glu130Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.286G>C
  hgvsp: ENSP00000380637.1:p.Glu96Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.360G>C
  hgvsp: ENSP00000414395.1:p.Glu121Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.286G>C
  hgvsp: ENSP00000412169.1:p.Glu96Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.383G>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.292G>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.395G>C
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*137G>C
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu96Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-32017810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017810
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017810
    reference: chr 22
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.281A>G
  hgvsp: ENSP00000412169.1:p.Gln94Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.95A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.390A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.383A>G
  hgvsp: ENSP00000338695.4:p.Gln128Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.434A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.287A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.355A>G
  hgvsp: ENSP00000414395.1:p.Gln119Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.281A>G
  hgvsp: ENSP00000380637.1:p.Gln94Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.383A>G
  hgvsp: ENSP00000391739.2:p.Gln128Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.281A>G
  hgvsp: ENSP00000371586.2:p.Gln94Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.378A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.281A>G
  hgvsp: ENSP00000266095.5:p.Gln94Arg
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*132A>G
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln94Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

22-32017813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017813
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017813
    reference: chr 22
allele count: 8
allele frequency: 6.609931421961497e-5
allele num: 121030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.380A>G
  hgvsp: ENSP00000338695.4:p.Asn127Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.284A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.278A>G
  hgvsp: ENSP00000371586.2:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.278A>G
  hgvsp: ENSP00000266095.5:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.375A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.278A>G
  hgvsp: ENSP00000412169.1:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.278A>G
  hgvsp: ENSP00000380637.1:p.Asn93Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.92A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.387A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.352A>G
  hgvsp: ENSP00000414395.1:p.Asn118Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.431A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*129A>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.380A>G
  hgvsp: ENSP00000391739.2:p.Asn127Ser
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Asn93Ser
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

22-32017819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017819
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017819
    reference: chr 22
allele count: 4
allele frequency: 3.30611300294244e-5
allele num: 120988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.272G>A
  hgvsp: ENSP00000266095.5:p.Arg91His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.374G>A
  hgvsp: ENSP00000391739.2:p.Arg125His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.346G>A
  hgvsp: ENSP00000414395.1:p.Arg116His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*123G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.374G>A
  hgvsp: ENSP00000338695.4:p.Arg125His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.272G>A
  hgvsp: ENSP00000380637.1:p.Arg91His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.369G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.272G>A
  hgvsp: ENSP00000412169.1:p.Arg91His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.381G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.86G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.272G>A
  hgvsp: ENSP00000371586.2:p.Arg91His
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.278G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.425G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25372
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg91His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

22-32017823-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017823
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017823
    reference: chr 22
allele count: 2
allele frequency: 1.653165812530997e-5
allele num: 120980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.421G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.268G>A
  hgvsp: ENSP00000412169.1:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.377G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.370G>A
  hgvsp: ENSP00000338695.4:p.Gly124Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.365G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*119G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.268G>A
  hgvsp: ENSP00000380637.1:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.268G>A
  hgvsp: ENSP00000371586.2:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.82G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.268G>A
  hgvsp: ENSP00000266095.5:p.Gly90Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.342G>A
  hgvsp: ENSP00000414395.1:p.Gly115Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.370G>A
  hgvsp: ENSP00000391739.2:p.Gly124Ser
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.274G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly90Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-32017831-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017831
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017831
    reference: chr 22
allele count: 5
allele frequency: 4.13517045172602e-5
allele num: 120914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.357G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.362G>A
  hgvsp: ENSP00000338695.4:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.260G>A
  hgvsp: ENSP00000380637.1:p.Arg87Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.266G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.74G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.334G>A
  hgvsp: ENSP00000414395.1:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.369G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.260G>A
  hgvsp: ENSP00000266095.5:p.Arg87Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*111G>A
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.260G>A
  hgvsp: ENSP00000371586.2:p.Arg87Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.362G>A
  hgvsp: ENSP00000391739.2:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.260G>A
  hgvsp: ENSP00000412169.1:p.Arg87Gln
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.413G>A
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg87Gln
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: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

22-32017832-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017832
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017832
    reference: chr 22
allele count: 2
allele frequency: 1.654122901331569e-5
allele num: 120910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.368C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*110C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.361C>T
  hgvsp: ENSP00000338695.4:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.259C>T
  hgvsp: ENSP00000412169.1:p.Arg87Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.259C>T
  hgvsp: ENSP00000266095.5:p.Arg87Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.73C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.333C>T
  hgvsp: ENSP00000414395.1:p.Arg112Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.361C>T
  hgvsp: ENSP00000391739.2:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.265C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.259C>T
  hgvsp: ENSP00000380637.1:p.Arg87Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.356C>T
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.259C>T
  hgvsp: ENSP00000371586.2:p.Arg87Trp
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.412C>T
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg87Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

22-32017834-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32017834
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 32017834
    reference: chr 22
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000473770
  gene symbol: PISD
  hgvsc: ENST00000473770.1:n.263C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000380637
  ensembl transcript: ENST00000397500
  gene symbol: PISD
  hgvsc: ENST00000397500.1:c.257C>G
  hgvsp: ENSP00000380637.1:p.Ser86Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000391739
  ensembl transcript: ENST00000439502
  gene symbol: PISD
  hgvsc: ENST00000439502.2:c.359C>G
  hgvsp: ENSP00000391739.2:p.Ser120Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000266095
  ensembl transcript: ENST00000266095
  gene symbol: PISD
  hgvsc: ENST00000266095.5:c.257C>G
  hgvsp: ENSP00000266095.5:p.Ser86Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000474017
  gene symbol: PISD
  hgvsc: ENST00000474017.1:n.354C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000396500
  ensembl transcript: ENST00000437808
  gene symbol: PISD
  hgvsc: ENST00000437808.1:c.*108C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000338695
  ensembl transcript: ENST00000336566
  gene symbol: PISD
  hgvsc: ENST00000336566.4:c.359C>G
  hgvsp: ENSP00000338695.4:p.Ser120Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000414395
  ensembl transcript: ENST00000435900
  gene symbol: PISD
  hgvsc: ENST00000435900.1:c.331C>G
  hgvsp: ENSP00000414395.1:p.Ser111Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000371586
  ensembl transcript: ENST00000382151
  gene symbol: PISD
  hgvsc: ENST00000382151.2:c.257C>G
  hgvsp: ENSP00000371586.2:p.Ser86Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000491342
  gene symbol: PISD
  hgvsc: ENST00000491342.1:n.71C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000241878
  ensembl protein: ENSP00000412169
  ensembl transcript: ENST00000422020
  gene symbol: PISD
  hgvsc: ENST00000422020.1:c.257C>G
  hgvsp: ENSP00000412169.1:p.Ser86Ter
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000478893
  gene symbol: PISD
  hgvsc: ENST00000478893.1:n.410C>G
  variant of: http://identifiers.org/hgnc/8999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000241878
  ensembl transcript: ENST00000460723
  gene symbol: PISD
  hgvsc: ENST00000460723.1:n.366C>G
  variant of: http://identifiers.org/hgnc/8999
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser86Ter
num of homozygotes: 0
population: South Asian
reference allele: G

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5616
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4782
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2578
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12565
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.665112561609165e-5
allele num: 60056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8682
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.417e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.002e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

VQSLOD
type: SiteQuality
SIO_000300: -1.917e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.883e1

MQRankSum
type: SiteQuality
SIO_000300: 8.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.66e-1

FS
type: SiteQuality
SIO_000300: 6.41e0

DP
type: SiteQuality
SIO_000300: 1.177825e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 27

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 892
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GenotypeQuality
all individuals: 1481
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5844
num of homozygotes: 0

African
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allele count: 26
allele frequency: 3.018342233573253e-3
allele num: 8614
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59834
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.920122887864823e-4
allele num: 10416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
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SIO_000300: 1.177051e6

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.0e-4

QD
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SIO_000300: 1.367e1

ClippingRankSum
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SIO_000300: -2.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 4.43e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 6

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

South Asian
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allele count: 3
allele frequency: 1.999200319872051e-4
allele num: 15006
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.028663381273258e-5
allele num: 59658
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.25e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 1.766e0

DP
type: SiteQuality
SIO_000300: 1.177285e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
all individuals: 453
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5856
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59800
num of homozygotes: 0

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

East Asian
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allele count: 2
allele frequency: 2.587991718426501e-4
allele num: 7728
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

MQ
type: SiteQuality
SIO_000300: 5.884e1

DP
type: SiteQuality
SIO_000300: 1.180313e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

BaseQRankSum
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SIO_000300: 2.75e0

InbreedingCoeff
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SIO_000300: -2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.312e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.708e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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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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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5840
num of homozygotes: 0

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

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

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

Latino
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: 7702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.674536990522121e-5
allele num: 59718
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
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MQRankSum
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FS
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QD
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BaseQRankSum
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SIO_000300: -6.166e0

DP
type: SiteQuality
SIO_000300: 1.183422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15090
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5838
num of homozygotes: 0

Latino
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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: 1
allele frequency: 1.295336787564767e-4
allele num: 7720
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59690
num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15114
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59770
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.292323597828896e-4
allele num: 7738
num of homozygotes: 0

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

Other
type: Population
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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

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

FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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SIO_000300: 2.96e-1

VQSLOD
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DP
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GenotypeDepth
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variant carriers: 1

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: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.667389201987528e-5
allele num: 59974
num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.199862e6

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 6.072e1

FS
type: SiteQuality
SIO_000300: 2.363e0

MQRankSum
type: SiteQuality
SIO_000300: 5.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 8.76e0

GenotypeDepth
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variant carriers: 77

GenotypeDepth
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variant carriers: 35

GenotypeDepth
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variant carriers: 13

GenotypeQuality
all individuals: 3960
bin: 5.25e1
variant carriers: 3

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 5.75e1
variant carriers: 4

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 705
bin: 8.75e1
variant carriers: 5

GenotypeQuality
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bin: 6.75e1
variant carriers: 3

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 4

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 833
bin: 9.25e1
variant carriers: 9

GenotypeQuality
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bin: 4.75e1
variant carriers: 6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 7

GenotypeQuality
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bin: 9.75e1
variant carriers: 552

GenotypeQuality
all individuals: 1682
bin: 8.25e1
variant carriers: 16

GenotypeQuality
all individuals: 14138
bin: 6.25e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 30
allele frequency: 4.785757585425773e-4
allele num: 62686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

African
type: Population
allele count: 532
allele frequency: 5.655964278120348e-2
allele num: 9406
num of homozygotes: 16

Latino
type: Population
allele count: 34
allele frequency: 3.129026320633168e-3
allele num: 10866
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.864743908503232e-4
allele num: 16088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.199040767386091e-3
allele num: 834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.85e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

DP
type: SiteQuality
SIO_000300: 1.324881e6

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

QD
type: SiteQuality
SIO_000300: 1.376e1

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 836
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GenotypeQuality
all individuals: 4775
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594133588394708e-5
allele num: 62730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.493e0

DP
type: SiteQuality
SIO_000300: 1.337566e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.05e1

GenotypeDepth
all individuals: 64
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 2380
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2999
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GenotypeQuality
all individuals: 5835
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.59073555612115e-5
allele num: 62864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16114
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

FS
type: SiteQuality
SIO_000300: 2.481e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.698e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.346505e6

GenotypeDepth
all individuals: 44
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 2401
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 546
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variant carriers: 0

GenotypeQuality
all individuals: 6391
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.488800398208064e-4
allele num: 8036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.583982766267503e-5
allele num: 63132
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 1.396431e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.055e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e0

FS
type: SiteQuality
SIO_000300: 4.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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
all individuals: 2970
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GenotypeQuality
all individuals: 885
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.73380250575946e-5
allele num: 63374
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.173708920187793e-3
allele num: 852
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

European (Finnish)
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allele count: 19
allele frequency: 3.096479791395045e-3
allele num: 6136
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

QD
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

FS
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 1.429934e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.480774001488464e-4
allele num: 8062
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.434152e6

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

BaseQRankSum
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SIO_000300: 3.78e0

ClippingRankSum
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SIO_000300: 9.19e-1

QD
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MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 20
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2035
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Other
type: Population
allele count: 0
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Latino
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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African
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DP
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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African
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South Asian
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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QD
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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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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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South Asian
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FS
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MQRankSum
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DP
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MQ
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QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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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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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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African
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Latino
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FS
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 44

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 41
allele frequency: 4.062623860483551e-3
allele num: 10092
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65488
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.506311360448808e-4
allele num: 11408
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
type: SiteQuality
SIO_000300: 1.488e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 1.56915e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.957e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 1.367e1

GenotypeDepth
all individuals: 453
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
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variant carriers: 0

GenotypeDepth
all individuals: 2532
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1072
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2601
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1908
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8560
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 997
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4076
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.592914663645549e-5
allele num: 65318
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.373e1

FS
type: SiteQuality
SIO_000300: 1.977e0

VQSLOD
type: SiteQuality
SIO_000300: 5.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e0

DP
type: SiteQuality
SIO_000300: 1.571932e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeDepth
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2553
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variant carriers: 1

GenotypeDepth
all individuals: 111
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variant carriers: 0

GenotypeDepth
all individuals: 257
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variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 679
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variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 2537
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variant carriers: 2

GenotypeQuality
all individuals: 391
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GenotypeQuality
all individuals: 745
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GenotypeQuality
all individuals: 4090
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variant carriers: 0

GenotypeQuality
all individuals: 1076
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variant carriers: 0

GenotypeQuality
all individuals: 236
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GenotypeQuality
all individuals: 495
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GenotypeQuality
all individuals: 31978
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GenotypeQuality
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 1931
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variant carriers: 0

GenotypeQuality
all individuals: 8662
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 1008
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variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.052596233096249e-5
allele num: 65518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.57557e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

FS
type: SiteQuality
SIO_000300: 3.19e0

QD
type: SiteQuality
SIO_000300: 1.431e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.901e1

GenotypeDepth
all individuals: 28
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 39
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variant carriers: 0

GenotypeDepth
all individuals: 36
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variant carriers: 0

GenotypeDepth
all individuals: 460
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variant carriers: 0

GenotypeDepth
all individuals: 1066
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variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 8711
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variant carriers: 0

GenotypeQuality
all individuals: 2551
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variant carriers: 14

GenotypeQuality
all individuals: 356
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variant carriers: 0

GenotypeQuality
all individuals: 194
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GenotypeQuality
all individuals: 3457
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 4121
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variant carriers: 0

GenotypeQuality
all individuals: 1881
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variant carriers: 0

GenotypeQuality
all individuals: 1078
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variant carriers: 0

GenotypeQuality
all individuals: 1013
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variant carriers: 0

GenotypeQuality
all individuals: 2632
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variant carriers: 0

GenotypeQuality
all individuals: 765
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variant carriers: 0

GenotypeQuality
all individuals: 32019
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variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.136360861869011e-4
allele num: 65532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.938382031405287e-5
allele num: 10062
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

DP
type: SiteQuality
SIO_000300: 1.576094e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 1.452e0

GenotypeDepth
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2541
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variant carriers: 0

GenotypeDepth
all individuals: 45
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variant carriers: 0

GenotypeDepth
all individuals: 255
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GenotypeDepth
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 2551
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variant carriers: 1

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2632
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 1013
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variant carriers: 0

GenotypeQuality
all individuals: 8711
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variant carriers: 0

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 32019
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variant carriers: 0

GenotypeQuality
all individuals: 270
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GenotypeQuality
all individuals: 765
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variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 356
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GenotypeQuality
all individuals: 3457
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GenotypeQuality
all individuals: 1078
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variant carriers: 0

GenotypeQuality
all individuals: 4121
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variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52597204419215e-5
allele num: 65532
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.108e0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

QD
type: SiteQuality
SIO_000300: 1.293e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

DP
type: SiteQuality
SIO_000300: 1.576094e6

FS
type: SiteQuality
SIO_000300: 1.452e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

GenotypeDepth
all individuals: 113
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 176
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GenotypeDepth
all individuals: 21
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GenotypeDepth
all individuals: 40
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GenotypeQuality
all individuals: 804
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GenotypeQuality
all individuals: 423
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GenotypeQuality
all individuals: 1775
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GenotypeQuality
all individuals: 1068
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variant carriers: 0

GenotypeQuality
all individuals: 159
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GenotypeQuality
all individuals: 2614
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variant carriers: 0

GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 348
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GenotypeQuality
all individuals: 122
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GenotypeQuality
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GenotypeQuality
all individuals: 618
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GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
all individuals: 8510
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GenotypeQuality
all individuals: 622
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 740
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 9.75e1
variant carriers: 11

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.052385406922357e-3
allele num: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053062221408072e-5
allele num: 65508
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.753e0

DP
type: SiteQuality
SIO_000300: 1.584277e6

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeDepth
all individuals: 112
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variant carriers: 0

GenotypeDepth
all individuals: 28
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variant carriers: 0

GenotypeDepth
all individuals: 477
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
all individuals: 612
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GenotypeQuality
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 430
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 750
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32033
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GenotypeQuality
all individuals: 295
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

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

South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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allele num: 66542
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Latino
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East Asian
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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: 1.50271992306074e-5
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num of homozygotes: 0

African
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East Asian
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Other
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FS
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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European (Non-Finnish)
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allele num: 66554
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East Asian
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European (Finnish)
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South Asian
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FS
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

Latino
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allele num: 11550
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East Asian
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allele count: 0
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Other
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11556
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South Asian
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European (Non-Finnish)
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African
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East Asian
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Other
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European (Finnish)
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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Other
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African
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European (Finnish)
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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East Asian
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Latino
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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DP
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QD
type: SiteQuality
SIO_000300: 1.195e1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
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SIO_000300: 1.6e0

FS
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MQ
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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DP
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SIO_000300: 1.622035e6

InbreedingCoeff
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SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.69e-2

QD
type: SiteQuality
SIO_000300: 1.558e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -4.697e0

ReadPosRankSum
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SIO_000300: -1.035e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: -3.98e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.622301e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 9.75e1
variant carriers: 5

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

Latino
type: Population
allele count: 3
allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
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SIO_000300: 8.500000000000001e-2

QD
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ClippingRankSum
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SIO_000300: -7.08e-1

VQSLOD
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SIO_000300: 2.53e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.622428e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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FS
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SIO_000300: 0.0e0

QD
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VQSLOD
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DP
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MQ
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ClippingRankSum
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SIO_000300: -1.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
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African
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South Asian
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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: 1.50154659299078e-5
allele num: 66598
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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DP
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 0

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

South Asian
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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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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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allele num: 8644
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Latino
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MQRankSum
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

East Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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Other
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South Asian
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 1.945525291828794e-4
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European (Non-Finnish)
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allele num: 66274
num of homozygotes: 0

East Asian
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allele frequency: 6.960556844547563e-4
allele num: 8620
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Latino
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European (Finnish)
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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QD
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele 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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European (Non-Finnish)
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allele num: 66344
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East Asian
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Other
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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African
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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MQ
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InbreedingCoeff
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FS
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DP
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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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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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 63210
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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SIO_000300: -2.941e0

ClippingRankSum
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QD
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
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allele count: 32
allele frequency: 5.062490112323999e-4
allele num: 63210
num of homozygotes: 0

East Asian
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allele frequency: 3.527751646284102e-4
allele num: 8504
num of homozygotes: 0

African
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allele count: 16
allele frequency: 1.744439598778892e-3
allele num: 9172
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 7
allele frequency: 1.202749140893471e-3
allele num: 5820
num of homozygotes: 0

Latino
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

Other
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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FS
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MQRankSum
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SIO_000300: 7.25e-1

MQ
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SIO_000300: 5.975e1

ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8630
num of homozygotes: 0

Other
type: Population
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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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num of homozygotes: 0

Latino
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allele num: 11566
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 9.189e0

QD
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.078e1

MQRankSum
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GenotypeDepth
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variant carriers: 0

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

African
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Latino
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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South Asian
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Latino
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Other
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.664749e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

GenotypeDepth
all individuals: 179
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variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1133
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 9.75e1
variant carriers: 2

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33628
bin: 6.25e1
variant carriers: 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: 3
allele frequency: 4.518072289156627e-5
allele num: 66400
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.065e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 1.66361e6

GenotypeDepth
all individuals: 381
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9281
bin: 6.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1.506069459923492e-5
allele num: 66398
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.206e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 1.253e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 1.663101e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.358e0

QD
type: SiteQuality
SIO_000300: 1.097e1

GenotypeDepth
all individuals: 582
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 1

GenotypeDepth
all individuals: 74
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variant carriers: 2

GenotypeDepth
all individuals: 179
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33642
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variant carriers: 0

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

GenotypeQuality
all individuals: 1132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 1218
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4400
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9268
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variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014318010550113e-5
allele num: 66350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 3.083e1

FS
type: SiteQuality
SIO_000300: 2.586e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.755e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.16e-1

DP
type: SiteQuality
SIO_000300: 1.662449e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

GenotypeDepth
all individuals: 119
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25356
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variant carriers: 0

GenotypeDepth
all individuals: 112
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variant carriers: 0

GenotypeDepth
all individuals: 52
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variant carriers: 0

GenotypeDepth
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

GenotypeQuality
all individuals: 2844
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507249871883761e-5
allele num: 66346
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

FS
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SIO_000300: 4.409e0

InbreedingCoeff
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DP
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ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.35e1

ClippingRankSum
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SIO_000300: 1.71e0

BaseQRankSum
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SIO_000300: -1.598e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.55e-1

GenotypeDepth
all individuals: 111
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variant carriers: 0

GenotypeDepth
all individuals: 179
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variant carriers: 0

GenotypeDepth
all individuals: 77
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variant carriers: 0

GenotypeDepth
all individuals: 72
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variant carriers: 0

GenotypeDepth
all individuals: 1134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3713
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 404
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 89
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GenotypeQuality
all individuals: 1132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 2845
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 4395
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

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