21-43241466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241466
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241466
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3115A>G
  hgvsp: ENSP00000415471.1:p.Met1039Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.2017A>G
  hgvsp: ENSP00000431410.1:p.Met673Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2188A>G
  hgvsp: ENSP00000408592.1:p.Met730Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3115A>G
  hgvsp: ENSP00000269844.3:p.Met1039Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2128A>G
  hgvsp: ENSP00000381556.1:p.Met710Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.2017A>G
  hgvsp: ENSP00000390245.2:p.Met673Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*468A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2077A>G
  hgvsp: ENSP00000444044.1:p.Met693Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*468A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5726
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met1039Val
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

21-43241470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241470
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241470
    reference: chr 21
allele count: 11
allele frequency: 9.060358460727464e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2073C>T
  hgvsp: ENST00000538201.1:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*464C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2184C>T
  hgvsp: ENST00000422911.1:c.2184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2124C>T
  hgvsp: ENST00000398548.1:c.2124C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.2013C>T
  hgvsp: ENST00000447207.2:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3111C>T
  hgvsp: ENST00000433067.1:c.3111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*464C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3111C>T
  hgvsp: ENST00000269844.3:c.3111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.2013C>T
  hgvsp: ENST00000447016.2:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala1037Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

21-43241473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241473
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241473
    reference: chr 21
allele count: 7
allele frequency: 5.765777638666952e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*461C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*461C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3108C>T
  hgvsp: ENST00000269844.3:c.3108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2181C>T
  hgvsp: ENST00000422911.1:c.2181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.2010C>T
  hgvsp: ENST00000447207.2:c.2010C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.2010C>T
  hgvsp: ENST00000447016.2:c.2010C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3108C>T
  hgvsp: ENST00000433067.1:c.3108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2121C>T
  hgvsp: ENST00000398548.1:c.2121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2070C>T
  hgvsp: ENST00000538201.1:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25587
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5715
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4416
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His1036His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

21-43241476-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241476
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241476
    reference: chr 21
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2118C>T
  hgvsp: ENST00000398548.1:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3105C>T
  hgvsp: ENST00000269844.3:c.3105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3105C>T
  hgvsp: ENST00000433067.1:c.3105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2178C>T
  hgvsp: ENST00000422911.1:c.2178C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2067C>T
  hgvsp: ENST00000538201.1:c.2067C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.2007C>T
  hgvsp: ENST00000447207.2:c.2007C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*458C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*458C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.2007C>T
  hgvsp: ENST00000447016.2:c.2007C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4419
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr1035Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

21-43241479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241479
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241479
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*455C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2115C>T
  hgvsp: ENST00000398548.1:c.2115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2175C>T
  hgvsp: ENST00000422911.1:c.2175C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*455C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.2004C>T
  hgvsp: ENST00000447207.2:c.2004C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2064C>T
  hgvsp: ENST00000538201.1:c.2064C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3102C>T
  hgvsp: ENST00000269844.3:c.3102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.2004C>T
  hgvsp: ENST00000447016.2:c.2004C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3102C>T
  hgvsp: ENST00000433067.1:c.3102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3049
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr1034Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

21-43241498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241498
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241498
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1985G>A
  hgvsp: ENSP00000431410.1:p.Arg662His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1985G>A
  hgvsp: ENSP00000390245.2:p.Arg662His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*436G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3083G>A
  hgvsp: ENSP00000269844.3:p.Arg1028His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2096G>A
  hgvsp: ENSP00000381556.1:p.Arg699His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3083G>A
  hgvsp: ENSP00000415471.1:p.Arg1028His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2045G>A
  hgvsp: ENSP00000444044.1:p.Arg682His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2156G>A
  hgvsp: ENSP00000408592.1:p.Arg719His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*436G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg1028His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

21-43241499-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241499
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241499
    reference: chr 21
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1984C>T
  hgvsp: ENSP00000390245.2:p.Arg662Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2155C>T
  hgvsp: ENSP00000408592.1:p.Arg719Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*435C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2044C>T
  hgvsp: ENSP00000444044.1:p.Arg682Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3082C>T
  hgvsp: ENSP00000415471.1:p.Arg1028Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2095C>T
  hgvsp: ENSP00000381556.1:p.Arg699Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1984C>T
  hgvsp: ENSP00000431410.1:p.Arg662Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3082C>T
  hgvsp: ENSP00000269844.3:p.Arg1028Cys
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*435C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1028Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

21-43241502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241502
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241502
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2092C>T
  hgvsp: ENSP00000381556.1:p.Arg698Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3079C>T
  hgvsp: ENSP00000415471.1:p.Arg1027Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1981C>T
  hgvsp: ENSP00000390245.2:p.Arg661Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2041C>T
  hgvsp: ENSP00000444044.1:p.Arg681Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2152C>T
  hgvsp: ENSP00000408592.1:p.Arg718Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1981C>T
  hgvsp: ENSP00000431410.1:p.Arg661Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3079C>T
  hgvsp: ENSP00000269844.3:p.Arg1027Trp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*432C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*432C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg1027Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

21-43241521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241521
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241521
    reference: chr 21
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1962T>C
  hgvsp: ENST00000447207.2:c.1962T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2133T>C
  hgvsp: ENST00000422911.1:c.2133T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*413T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2073T>C
  hgvsp: ENST00000398548.1:c.2073T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*413T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3060T>C
  hgvsp: ENST00000269844.3:c.3060T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2022T>C
  hgvsp: ENST00000538201.1:c.2022T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3060T>C
  hgvsp: ENST00000433067.1:c.3060T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1962T>C
  hgvsp: ENST00000447016.2:c.1962T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr1020Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

21-43241522-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241522
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241523
    reference: chr 21
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3058dupT
  hgvsp: ENSP00000415471.1:p.Tyr1020LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1960dupT
  hgvsp: ENSP00000390245.2:p.Tyr654LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3058dupT
  hgvsp: ENSP00000269844.3:p.Tyr1020LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*411dupT
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2020dupT
  hgvsp: ENSP00000444044.1:p.Tyr674LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2071dupT
  hgvsp: ENSP00000381556.1:p.Tyr691LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2131dupT
  hgvsp: ENSP00000408592.1:p.Tyr711LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*411dupT
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1960dupT
  hgvsp: ENSP00000431410.1:p.Tyr654LeufsTer25
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr1020LeufsTer25
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

21-43241524-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241524
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241524
    reference: chr 21
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1959C>T
  hgvsp: ENST00000447207.2:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2130C>T
  hgvsp: ENST00000422911.1:c.2130C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3057C>T
  hgvsp: ENST00000433067.1:c.3057C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*410C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3057C>T
  hgvsp: ENST00000269844.3:c.3057C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*410C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2019C>T
  hgvsp: ENST00000538201.1:c.2019C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1959C>T
  hgvsp: ENST00000447016.2:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2070C>T
  hgvsp: ENST00000398548.1:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30702
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly1019Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/21-43241525-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241525
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241525
    reference: chr 21
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3056G>T
  hgvsp: ENSP00000415471.1:p.Gly1019Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1958G>T
  hgvsp: ENSP00000431410.1:p.Gly653Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1958G>T
  hgvsp: ENSP00000390245.2:p.Gly653Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*409G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2018G>T
  hgvsp: ENSP00000444044.1:p.Gly673Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3056G>T
  hgvsp: ENSP00000269844.3:p.Gly1019Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*409G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2069G>T
  hgvsp: ENSP00000381556.1:p.Gly690Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2129G>T
  hgvsp: ENSP00000408592.1:p.Gly710Val
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3464
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly1019Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

21-43241533-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241533
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241533
    reference: chr 21
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3048G>A
  hgvsp: ENST00000269844.3:c.3048G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2061G>A
  hgvsp: ENST00000398548.1:c.2061G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1950G>A
  hgvsp: ENST00000447016.2:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2121G>A
  hgvsp: ENST00000422911.1:c.2121G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3048G>A
  hgvsp: ENST00000433067.1:c.3048G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1950G>A
  hgvsp: ENST00000447207.2:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2010G>A
  hgvsp: ENST00000538201.1:c.2010G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*401G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*401G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30700
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys1016Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

21-43241535-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241535
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241535
    reference: chr 21
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3046A>C
  hgvsp: ENSP00000415471.1:p.Lys1016Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1948A>C
  hgvsp: ENSP00000431410.1:p.Lys650Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1948A>C
  hgvsp: ENSP00000390245.2:p.Lys650Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2119A>C
  hgvsp: ENSP00000408592.1:p.Lys707Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3046A>C
  hgvsp: ENSP00000269844.3:p.Lys1016Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*399A>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2059A>C
  hgvsp: ENSP00000381556.1:p.Lys687Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*399A>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2008A>C
  hgvsp: ENSP00000444044.1:p.Lys670Gln
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys1016Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

21-43241540-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241540
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241540
    reference: chr 21
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2114T>C
  hgvsp: ENSP00000408592.1:p.Val705Ala
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*394T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3041T>C
  hgvsp: ENSP00000269844.3:p.Val1014Ala
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1943T>C
  hgvsp: ENSP00000390245.2:p.Val648Ala
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2003T>C
  hgvsp: ENSP00000444044.1:p.Val668Ala
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3041T>C
  hgvsp: ENSP00000415471.1:p.Val1014Ala
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*394T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1943T>C
  hgvsp: ENSP00000431410.1:p.Val648Ala
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2054T>C
  hgvsp: ENSP00000381556.1:p.Val685Ala
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val1014Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-43241541-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241541
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241541
    reference: chr 21
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2113G>T
  hgvsp: ENSP00000408592.1:p.Val705Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1942G>T
  hgvsp: ENSP00000431410.1:p.Val648Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2053G>T
  hgvsp: ENSP00000381556.1:p.Val685Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2002G>T
  hgvsp: ENSP00000444044.1:p.Val668Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3040G>T
  hgvsp: ENSP00000269844.3:p.Val1014Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1942G>T
  hgvsp: ENSP00000390245.2:p.Val648Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*393G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*393G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3040G>T
  hgvsp: ENSP00000415471.1:p.Val1014Leu
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val1014Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

21-43241541-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241541
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241541
    reference: chr 21
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3040G>A
  hgvsp: ENSP00000415471.1:p.Val1014Met
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2002G>A
  hgvsp: ENSP00000444044.1:p.Val668Met
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*393G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3040G>A
  hgvsp: ENSP00000269844.3:p.Val1014Met
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1942G>A
  hgvsp: ENSP00000390245.2:p.Val648Met
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1942G>A
  hgvsp: ENSP00000431410.1:p.Val648Met
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2053G>A
  hgvsp: ENSP00000381556.1:p.Val685Met
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*393G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2113G>A
  hgvsp: ENSP00000408592.1:p.Val705Met
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3041
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val1014Met
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

21-43241542-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241542
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241542
    reference: chr 21
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.2001G>C
  hgvsp: ENSP00000444044.1:p.Glu667Asp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1941G>C
  hgvsp: ENSP00000390245.2:p.Glu647Asp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*392G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2052G>C
  hgvsp: ENSP00000381556.1:p.Glu684Asp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*392G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3039G>C
  hgvsp: ENSP00000415471.1:p.Glu1013Asp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3039G>C
  hgvsp: ENSP00000269844.3:p.Glu1013Asp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2112G>C
  hgvsp: ENSP00000408592.1:p.Glu704Asp
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1941G>C
  hgvsp: ENSP00000431410.1:p.Glu647Asp
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1013Asp
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

21-43241547-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241547
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241547
    reference: chr 21
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1996A>G
  hgvsp: ENSP00000444044.1:p.Met666Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3034A>G
  hgvsp: ENSP00000269844.3:p.Met1012Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*387A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2047A>G
  hgvsp: ENSP00000381556.1:p.Met683Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3034A>G
  hgvsp: ENSP00000415471.1:p.Met1012Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1936A>G
  hgvsp: ENSP00000390245.2:p.Met646Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2107A>G
  hgvsp: ENSP00000408592.1:p.Met703Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*387A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1936A>G
  hgvsp: ENSP00000431410.1:p.Met646Val
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.520A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met1012Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/21-43241549-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241549
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241549
    reference: chr 21
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*385T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1934T>G
  hgvsp: ENSP00000431410.1:p.Ile645Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1934T>G
  hgvsp: ENSP00000390245.2:p.Ile645Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3032T>G
  hgvsp: ENSP00000269844.3:p.Ile1011Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*385T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3032T>G
  hgvsp: ENSP00000415471.1:p.Ile1011Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2045T>G
  hgvsp: ENSP00000381556.1:p.Ile682Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.518T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1994T>G
  hgvsp: ENSP00000444044.1:p.Ile665Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2105T>G
  hgvsp: ENSP00000408592.1:p.Ile702Ser
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile1011Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

21-43241549-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241549
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241549
    reference: chr 21
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2045T>C
  hgvsp: ENSP00000381556.1:p.Ile682Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3032T>C
  hgvsp: ENSP00000415471.1:p.Ile1011Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1994T>C
  hgvsp: ENSP00000444044.1:p.Ile665Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3032T>C
  hgvsp: ENSP00000269844.3:p.Ile1011Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*385T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2105T>C
  hgvsp: ENSP00000408592.1:p.Ile702Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1934T>C
  hgvsp: ENSP00000390245.2:p.Ile645Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.518T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1934T>C
  hgvsp: ENSP00000431410.1:p.Ile645Thr
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*385T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile1011Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/21-43241565-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241565
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241565
    reference: chr 21
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*369G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3016G>T
  hgvsp: ENSP00000269844.3:p.Glu1006Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1978G>T
  hgvsp: ENSP00000444044.1:p.Glu660Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1918G>T
  hgvsp: ENSP00000431410.1:p.Glu640Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2029G>T
  hgvsp: ENSP00000381556.1:p.Glu677Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3016G>T
  hgvsp: ENSP00000415471.1:p.Glu1006Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2089G>T
  hgvsp: ENSP00000408592.1:p.Glu697Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1918G>T
  hgvsp: ENSP00000390245.2:p.Glu640Ter
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*369G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.502G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu1006Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ

21-43241565-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241565
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241565
    reference: chr 21
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3016G>C
  hgvsp: ENSP00000269844.3:p.Glu1006Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2089G>C
  hgvsp: ENSP00000408592.1:p.Glu697Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3016G>C
  hgvsp: ENSP00000415471.1:p.Glu1006Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1918G>C
  hgvsp: ENSP00000390245.2:p.Glu640Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1978G>C
  hgvsp: ENSP00000444044.1:p.Glu660Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2029G>C
  hgvsp: ENSP00000381556.1:p.Glu677Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*369G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1918G>C
  hgvsp: ENSP00000431410.1:p.Glu640Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.502G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*369G>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu1006Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

21-43241573-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241573
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241573
    reference: chr 21
allele count: 3
allele frequency: 2.474267616785431e-5
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*361G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1910G>A
  hgvsp: ENSP00000390245.2:p.Arg637Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3008G>A
  hgvsp: ENSP00000415471.1:p.Arg1003Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.494G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3008G>A
  hgvsp: ENSP00000269844.3:p.Arg1003Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1970G>A
  hgvsp: ENSP00000444044.1:p.Arg657Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2021G>A
  hgvsp: ENSP00000381556.1:p.Arg674Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2081G>A
  hgvsp: ENSP00000408592.1:p.Arg694Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*361G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1910G>A
  hgvsp: ENSP00000431410.1:p.Arg637Gln
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1003Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

21-43241575-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241575
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241575
    reference: chr 21
allele count: 19
allele frequency: 1.567139557901683e-4
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3006C>A
  hgvsp: ENST00000269844.3:c.3006C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2019C>A
  hgvsp: ENST00000398548.1:c.2019C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1908C>A
  hgvsp: ENST00000447016.2:c.1908C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1968C>A
  hgvsp: ENST00000538201.1:c.1968C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3006C>A
  hgvsp: ENST00000433067.1:c.3006C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.492C>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*359C>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2079C>A
  hgvsp: ENST00000422911.1:c.2079C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*359C>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1908C>A
  hgvsp: ENST00000447207.2:c.1908C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25542
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly1002Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

21-43241577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241577
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241577
    reference: chr 21
allele count: 5
allele frequency: 4.124799947202561e-5
allele num: 121218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2017G>A
  hgvsp: ENSP00000381556.1:p.Gly673Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3004G>A
  hgvsp: ENSP00000269844.3:p.Gly1002Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.490G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*357G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3004G>A
  hgvsp: ENSP00000415471.1:p.Gly1002Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2077G>A
  hgvsp: ENSP00000408592.1:p.Gly693Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1906G>A
  hgvsp: ENSP00000390245.2:p.Gly636Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1966G>A
  hgvsp: ENSP00000444044.1:p.Gly656Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1906G>A
  hgvsp: ENSP00000431410.1:p.Gly636Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*357G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly1002Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

21-43241578-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241578
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241578
    reference: chr 21
allele count: 1078
allele frequency: 8.893215417106652e-3
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*356C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1905C>T
  hgvsp: ENST00000447016.2:c.1905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.3003C>T
  hgvsp: ENST00000433067.1:c.3003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1965C>T
  hgvsp: ENST00000538201.1:c.1965C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*356C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.3003C>T
  hgvsp: ENST00000269844.3:c.3003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2076C>T
  hgvsp: ENST00000422911.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1905C>T
  hgvsp: ENST00000447207.2:c.1905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.489C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2016C>T
  hgvsp: ENST00000398548.1:c.2016C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 16816
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 4.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 3.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 25504
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe1001Phe
num of homozygotes: 47
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

21-43241586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241586
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241586
    reference: chr 21
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995C>T
  hgvsp: ENSP00000415471.1:p.Leu999Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068C>T
  hgvsp: ENSP00000408592.1:p.Leu690Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008C>T
  hgvsp: ENSP00000381556.1:p.Leu670Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897C>T
  hgvsp: ENSP00000390245.2:p.Leu633Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957C>T
  hgvsp: ENSP00000444044.1:p.Leu653Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995C>T
  hgvsp: ENSP00000269844.3:p.Leu999Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897C>T
  hgvsp: ENSP00000431410.1:p.Leu633Phe
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu999Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

21-43241590-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241590
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241590
    reference: chr 21
allele count: 49
allele frequency: 4.047044831345601e-4
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-4G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-4G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16904
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2995-4G>A
num of homozygotes: 2
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

21-43241591-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241591
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241591
    reference: chr 21
allele count: 27
allele frequency: 2.230851854912005e-4
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-5C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-5C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16857
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: c.2995-5C>T
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

21-43241600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241600
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241600
    reference: chr 21
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-14C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-14C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16584
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

21-43241601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241601
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241601
    reference: chr 21
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-15C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-15C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

21-43241604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241604
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241604
    reference: chr 21
allele count: 2
allele frequency: 1.655546909921693e-5
allele num: 120806
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-18T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-18T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10224
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

21-43241606-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241606
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241606
    reference: chr 21
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-20C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-20C>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

21-43241621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241621
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241621
    reference: chr 21
allele count: 2
allele frequency: 1.663755095249979e-5
allele num: 120210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-35G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-35G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20774
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2591
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

21-43241622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241622
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241622
    reference: chr 21
allele count: 60
allele frequency: 5.001667222407469e-4
allele num: 119960
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-36C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-36C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20878
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

21-43241628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241628
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241628
    reference: chr 21
allele count: 4
allele frequency: 3.33672567109895e-5
allele num: 119878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-42C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-42C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16079
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3719
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

21-43241629-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241629
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241629
    reference: chr 21
allele count: 9
allele frequency: 7.50650563821979e-5
allele num: 119896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-43C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-43C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10654
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16119
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9181
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4675
  bin: 9.75e1
  variant carriers: 9
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

21-43241634-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43241634
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43241634
    reference: chr 21
allele count: 1
allele frequency: 8.369041242635244e-6
allele num: 119488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2995-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*348-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2008-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1957-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1897-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*348-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2995-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.481-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1897-48A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2068-48A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13834
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum

21-43242212-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242212
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242212
    reference: chr 21
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+47G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+47G>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

21-43242217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242217
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242217
    reference: chr 21
allele count: 1156
allele frequency: 9.5329199102784e-3
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+42G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+42G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 7.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 4.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 6.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 6.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 5.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 5.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 8.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 7.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 44574
  bin: 9.75e1
  variant carriers: 1108
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 46
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

21-43242219-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242219
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242219
    reference: chr 21
allele count: 1188
allele frequency: 9.796645391123645e-3
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+40G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+40G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 4.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 9.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 5.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 4.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 6.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 6.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 5.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 7.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 7.25e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 46
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

21-43242224-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242224
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242224
    reference: chr 21
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+35C>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+35C>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44422
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

21-43242229-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242229
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242229
    reference: chr 21
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+30G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+30G>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

21-43242236-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242236
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242236
    reference: chr 21
allele count: 532
allele frequency: 4.393208693928783e-3
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+23T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+23T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 6.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 6.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 7.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 5.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 5.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 7.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 9.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 5
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

21-43242236-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242236
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242236
    reference: chr 21
allele count: 66
allele frequency: 5.450221312016913e-4
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+23T>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+23T>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/21-43242237-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242237
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242237
    reference: chr 21
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+22G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+22G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/21-43242238-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242238
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242238
    reference: chr 21
allele count: 4
allele frequency: 3.298207424264912e-5
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+21G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+21G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3926
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

21-43242238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242238
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242238
    reference: chr 21
allele count: 13
allele frequency: 1.071917412886096e-4
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+21G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+21G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3926
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

21-43242239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242239
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242239
    reference: chr 21
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+20C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+20C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-43242240-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242240
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242240
    reference: chr 21
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+19G>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+19G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

21-43242241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242241
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242241
    reference: chr 21
allele count: 1154
allele frequency: 9.514543895521404e-3
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+18C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+18C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 6.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 5.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 6.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 8.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 6562
  bin: 5.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 4.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 9.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 7.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 8.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 3.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 47
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

21-43242243-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242243
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242243
    reference: chr 21
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+16C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+16C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/21-43242247-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242247
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242247
    reference: chr 21
allele count: 16
allele frequency: 1.320371684629223e-4
allele num: 121178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+12T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+12T>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/21-43242248-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242248
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242248
    reference: chr 21
allele count: 1
allele frequency: 8.422754914677492e-6
allele num: 118726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+11T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+11T>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

21-43242248-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242248
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242248
    reference: chr 21
allele count: 1
allele frequency: 8.422754914677492e-6
allele num: 118726
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+11T>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+11T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43304
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

21-43242251-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242251
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242251
    reference: chr 21
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+8G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+8G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2994+8G>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

21-43242252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242252
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242252
    reference: chr 21
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+7C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+7C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.2994+7C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

21-43242253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242253
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242253
    reference: chr 21
allele count: 22
allele frequency: 1.812967663249497e-4
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.480+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2007+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1896+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*347+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2994+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2067+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1956+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2994+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*347+6G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1896+6G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2994+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-43242264-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242264
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242264
    reference: chr 21
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2002T>G
  hgvsp: ENSP00000381556.1:p.Cys668Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*342T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1951T>G
  hgvsp: ENSP00000444044.1:p.Cys651Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1891T>G
  hgvsp: ENSP00000390245.2:p.Cys631Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2989T>G
  hgvsp: ENSP00000415471.1:p.Cys997Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2062T>G
  hgvsp: ENSP00000408592.1:p.Cys688Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*342T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.475T>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1891T>G
  hgvsp: ENSP00000431410.1:p.Cys631Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2989T>G
  hgvsp: ENSP00000269844.3:p.Cys997Gly
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys997Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

21-43242266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242266
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242266
    reference: chr 21
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1889G>A
  hgvsp: ENSP00000390245.2:p.Arg630Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2060G>A
  hgvsp: ENSP00000408592.1:p.Arg687Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1949G>A
  hgvsp: ENSP00000444044.1:p.Arg650Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2987G>A
  hgvsp: ENSP00000415471.1:p.Arg996Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.2000G>A
  hgvsp: ENSP00000381556.1:p.Arg667Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.473G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1889G>A
  hgvsp: ENSP00000431410.1:p.Arg630Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2987G>A
  hgvsp: ENSP00000269844.3:p.Arg996Gln
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*340G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*340G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg996Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

21-43242283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242283
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242283
    reference: chr 21
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.456C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1872C>T
  hgvsp: ENST00000447207.2:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2970C>T
  hgvsp: ENST00000269844.3:c.2970C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2970C>T
  hgvsp: ENST00000433067.1:c.2970C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1983C>T
  hgvsp: ENST00000398548.1:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2043C>T
  hgvsp: ENST00000422911.1:c.2043C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1932C>T
  hgvsp: ENST00000538201.1:c.1932C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1872C>T
  hgvsp: ENST00000447016.2:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*323C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*323C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His990His
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

21-43242293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242293
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242293
    reference: chr 21
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1973C>T
  hgvsp: ENSP00000381556.1:p.Ser658Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*313C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.446C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1862C>T
  hgvsp: ENSP00000390245.2:p.Ser621Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2033C>T
  hgvsp: ENSP00000408592.1:p.Ser678Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1922C>T
  hgvsp: ENSP00000444044.1:p.Ser641Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2960C>T
  hgvsp: ENSP00000269844.3:p.Ser987Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*313C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2960C>T
  hgvsp: ENSP00000415471.1:p.Ser987Leu
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1862C>T
  hgvsp: ENSP00000431410.1:p.Ser621Leu
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser987Leu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

21-43242304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242304
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242304
    reference: chr 21
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2949G>A
  hgvsp: ENST00000269844.3:c.2949G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2022G>A
  hgvsp: ENST00000422911.1:c.2022G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1962G>A
  hgvsp: ENST00000398548.1:c.1962G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1851G>A
  hgvsp: ENST00000447016.2:c.1851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.435G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2949G>A
  hgvsp: ENST00000433067.1:c.2949G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1911G>A
  hgvsp: ENST00000538201.1:c.1911G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*302G>A
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1851G>A
  hgvsp: ENST00000447207.2:c.1851G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*302G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu983Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

21-43242305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242305
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242305
    reference: chr 21
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2948A>G
  hgvsp: ENSP00000415471.1:p.Glu983Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1850A>G
  hgvsp: ENSP00000390245.2:p.Glu617Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1910A>G
  hgvsp: ENSP00000444044.1:p.Glu637Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1961A>G
  hgvsp: ENSP00000381556.1:p.Glu654Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*301A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*301A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.434A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1850A>G
  hgvsp: ENSP00000431410.1:p.Glu617Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2948A>G
  hgvsp: ENSP00000269844.3:p.Glu983Gly
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2021A>G
  hgvsp: ENSP00000408592.1:p.Glu674Gly
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu983Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

21-43242307-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242307
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242307
    reference: chr 21
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.432C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*299C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2019C>T
  hgvsp: ENST00000422911.1:c.2019C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1848C>T
  hgvsp: ENST00000447016.2:c.1848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1959C>T
  hgvsp: ENST00000398548.1:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1908C>T
  hgvsp: ENST00000538201.1:c.1908C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*299C>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2946C>T
  hgvsp: ENST00000433067.1:c.2946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1848C>T
  hgvsp: ENST00000447207.2:c.1848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2946C>T
  hgvsp: ENST00000269844.3:c.2946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp982Asp
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

21-43242314-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242314
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242314
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1841A>T
  hgvsp: ENSP00000431410.1:p.Asn614Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2939A>T
  hgvsp: ENSP00000269844.3:p.Asn980Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2012A>T
  hgvsp: ENSP00000408592.1:p.Asn671Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1901A>T
  hgvsp: ENSP00000444044.1:p.Asn634Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1841A>T
  hgvsp: ENSP00000390245.2:p.Asn614Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2939A>T
  hgvsp: ENSP00000415471.1:p.Asn980Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1952A>T
  hgvsp: ENSP00000381556.1:p.Asn651Ile
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*292A>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*292A>T
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.425A>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn980Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

21-43242314-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242314
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242314
    reference: chr 21
allele count: 4
allele frequency: 3.294675803900896e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1901A>G
  hgvsp: ENSP00000444044.1:p.Asn634Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1841A>G
  hgvsp: ENSP00000390245.2:p.Asn614Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*292A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2012A>G
  hgvsp: ENSP00000408592.1:p.Asn671Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*292A>G
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2939A>G
  hgvsp: ENSP00000415471.1:p.Asn980Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1841A>G
  hgvsp: ENSP00000431410.1:p.Asn614Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2939A>G
  hgvsp: ENSP00000269844.3:p.Asn980Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1952A>G
  hgvsp: ENSP00000381556.1:p.Asn651Ser
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.425A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn980Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

21-43242318-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43242318
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43242318
    reference: chr 21
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.2008G>C
  hgvsp: ENSP00000408592.1:p.Asp670His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.2935G>C
  hgvsp: ENSP00000269844.3:p.Asp979His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000396943
  ensembl transcript: ENST00000449395
  gene symbol: PRDM15
  hgvsc: ENST00000449395.1:c.*288G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsc: ENST00000433067.1:c.2935G>C
  hgvsp: ENSP00000415471.1:p.Asp979His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000390245
  ensembl transcript: ENST00000447207
  gene symbol: PRDM15
  hgvsc: ENST00000447207.2:c.1837G>C
  hgvsp: ENSP00000390245.2:p.Asp613His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.1897G>C
  hgvsp: ENSP00000444044.1:p.Asp633His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.1948G>C
  hgvsp: ENSP00000381556.1:p.Asp650His
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000387958
  ensembl transcript: ENST00000441787
  gene symbol: PRDM15
  hgvsc: ENST00000441787.1:c.*288G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141956
  ensembl transcript: ENST00000491486
  gene symbol: PRDM15
  hgvsc: ENST00000491486.1:n.421G>C
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000431410
  ensembl transcript: ENST00000447016
  gene symbol: PRDM15
  hgvsc: ENST00000447016.2:c.1837G>C
  hgvsp: ENSP00000431410.1:p.Asp613His
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp979His
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3045
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30667
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4417
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10516
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.724e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 5.78e-1

DP
type: SiteQuality
SIO_000300: 1.923732e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.041e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.413e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30667
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4416
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5725
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.492208103572285e-5
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

DP
type: SiteQuality
SIO_000300: 1.923645e6

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 7.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30672
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.922296e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10516
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5708
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 1.921689e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

FS
type: SiteQuality
SIO_000300: 4.096e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.095e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

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

GenotypeQuality
all individuals: 3472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10517
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5706
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1612
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30685
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1233
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4419
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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MQ
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FS
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QD
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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Other
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South Asian
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African
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MQ
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FS
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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African
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South Asian
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European (Non-Finnish)
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MQ
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MQRankSum
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DP
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VQSLOD
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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Other
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East Asian
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Latino
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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East Asian
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Latino
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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VQSLOD
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FS
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MQ
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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South Asian
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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DP
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MQRankSum
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QD
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

East 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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Other
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BaseQRankSum
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MQ
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SIO_000300: 5.912e1

FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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VQSLOD
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ClippingRankSum
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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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variant carriers: 0

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
allele num: 6614
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
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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 num: 66728
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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InbreedingCoeff
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VQSLOD
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FS
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QD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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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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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66724
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10402
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Latino
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allele frequency: 0.0e0
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South Asian
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QD
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FS
type: SiteQuality
SIO_000300: 8.093e0

InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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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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variant carriers: 1

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: 1
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allele num: 66722
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Latino
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num of homozygotes: 0

East Asian
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Other
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South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
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BaseQRankSum
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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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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num of homozygotes: 0

Other
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DP
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.054e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

FS
type: SiteQuality
SIO_000300: 1.225e0

DP
type: SiteQuality
SIO_000300: 1.918744e6

QD
type: SiteQuality
SIO_000300: 1.445e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

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

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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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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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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.131e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.15e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.45e-1

DP
type: SiteQuality
SIO_000300: 1.916925e6

FS
type: SiteQuality
SIO_000300: 9.510999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.916925e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.131e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.15e1

FS
type: SiteQuality
SIO_000300: 9.510999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.45e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10466
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.94e-1

DP
type: SiteQuality
SIO_000300: 1.914261e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.599e0

QD
type: SiteQuality
SIO_000300: 1.167e1

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 3017
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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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bin: 9.75e1
variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10464
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GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 17
allele frequency: 1.635873749037721e-3
allele num: 10392
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 6.44e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

BaseQRankSum
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SIO_000300: -3.034e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 1.913793e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5612
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1222
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.041362530413625e-4
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502341217433065e-5
allele num: 66632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.911788e6

QD
type: SiteQuality
SIO_000300: 1.049e1

VQSLOD
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SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 1.413e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.156e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

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
all individuals: 5
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GenotypeQuality
all individuals: 5755
bin: 9.75e1
variant carriers: 1027

Latino
type: Population
allele count: 58
allele frequency: 5.016433143054835e-3
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.424242424242424e-4
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 39
allele frequency: 5.852692238429677e-4
allele num: 66636
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.424778761061947e-3
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 973
allele frequency: 9.368380512227999e-2
allele num: 10386
num of homozygotes: 47

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.48e0

FS
type: SiteQuality
SIO_000300: 1.346e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.52e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

DP
type: SiteQuality
SIO_000300: 1.923435e6

QD
type: SiteQuality
SIO_000300: 1.439e1

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
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
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GenotypeQuality
all individuals: 1589
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GenotypeQuality
all individuals: 1223
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GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.651e0

DP
type: SiteQuality
SIO_000300: 1.879163e6

FS
type: SiteQuality
SIO_000300: 3.774e0

VQSLOD
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 1.048e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4878
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 3022
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1215
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 3.857280617164899e-4
allele num: 10370
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502403846153846e-5
allele num: 66560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 40
allele frequency: 2.425712553062462e-3
allele num: 16490
num of homozygotes: 2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

DP
type: SiteQuality
SIO_000300: 1.876592e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.15e-2

QD
type: SiteQuality
SIO_000300: 1.336e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 30704
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4829
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 1212
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10508
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3426
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 26
allele frequency: 2.508199884236928e-3
allele num: 10366
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.873245e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.434e1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

GenotypeQuality
all individuals: 30500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4780
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3358
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2971
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-2

DP
type: SiteQuality
SIO_000300: 1.860999e6

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30495
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10315
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4776
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 749
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.185e0

DP
type: SiteQuality
SIO_000300: 1.85926e6

GenotypeQuality
all individuals: 892
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1557
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4768
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4244
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010687942194791e-5
allele num: 66430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.587e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

DP
type: SiteQuality
SIO_000300: 1.852541e6

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 1036
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4211
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 4757
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
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variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 29928
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506250941406838e-5
allele num: 66390
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.772e0

MQRankSum
type: SiteQuality
SIO_000300: -1.289e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: -3.097e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

QD
type: SiteQuality
SIO_000300: 1.401e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.845376e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.447e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

GenotypeQuality
all individuals: 8598
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
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variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 651
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4714
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1131
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.093102607847916e-5
allele num: 16412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 1.737435e6

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 2640
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4732
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 3679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8329
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 5.242922055225446e-4
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 8.031763350912287e-4
allele num: 65988
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.627e0

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.733211e6

QD
type: SiteQuality
SIO_000300: 1.299e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

GenotypeQuality
all individuals: 1482
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2490
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variant carriers: 0

GenotypeQuality
all individuals: 4674
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.067040800849386e-5
allele num: 65930
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: 10250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.73e0

VQSLOD
type: SiteQuality
SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 1.653387e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

QD
type: SiteQuality
SIO_000300: 1.331e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17518
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2387
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variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.58334091667425e-5
allele num: 65934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.677268475210477e-4
allele num: 6414
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.304e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 7.323e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.563e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.652011e6

GenotypeQuality
all individuals: 5285
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
all individuals: 13233
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521236460995497e-5
allele num: 65736
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.609e0

DP
type: SiteQuality
SIO_000300: 1.624143e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.04e1

MQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

GenotypeQuality
all individuals: 1439
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 3304
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GenotypeQuality
all individuals: 44425
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variant carriers: 1

GenotypeQuality
all individuals: 2
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 126
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GenotypeQuality
all individuals: 2018
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GenotypeQuality
all individuals: 1515
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variant carriers: 0

GenotypeQuality
all individuals: 151
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variant carriers: 0

GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 270
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variant carriers: 0

GenotypeQuality
all individuals: 143
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variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

QD
type: SiteQuality
SIO_000300: 1.746e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.164e0

VQSLOD
type: SiteQuality
SIO_000300: -1.016e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.260804e6

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
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variant carriers: 0

GenotypeQuality
all individuals: 1509
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variant carriers: 0

GenotypeQuality
all individuals: 2258
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 108
bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 226
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variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 82
allele frequency: 7.083621285418107e-3
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 991
allele frequency: 9.530678976726294e-2
allele num: 10398
num of homozygotes: 46

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 8.103484498334283e-4
allele num: 66638
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.455957291919437e-3
allele num: 16484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.316e-1

FS
type: SiteQuality
SIO_000300: 2.054e0

MQ
type: SiteQuality
SIO_000300: 5.803e1

DP
type: SiteQuality
SIO_000300: 3.267134e6

QD
type: SiteQuality
SIO_000300: 1.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.87e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
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GenotypeQuality
all individuals: 145
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GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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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: 1140

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1431
bin: 8.75e1
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GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 39
allele frequency: 2.365930599369085e-3
allele num: 16484
num of homozygotes: 0

Latino
type: Population
allele count: 90
allele frequency: 7.77336327517706e-3
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.622516556291391e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 993
allele frequency: 9.551750673335899e-2
allele num: 10396
num of homozygotes: 46

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 59
allele frequency: 8.853541416566626e-4
allele num: 66640
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.518e0

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

FS
type: SiteQuality
SIO_000300: 2.054e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 5.808e1

DP
type: SiteQuality
SIO_000300: 3.269314e6

QD
type: SiteQuality
SIO_000300: 1.915e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2289
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.096e0

VQSLOD
type: SiteQuality
SIO_000300: -2.101e0

MQRankSum
type: SiteQuality
SIO_000300: -1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.270091e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.386e0

MQ
type: SiteQuality
SIO_000300: 5.799e1

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
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GenotypeQuality
all individuals: 1452
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 100
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GenotypeQuality
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GenotypeQuality
all individuals: 3875
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 70
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2072
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GenotypeQuality
all individuals: 2029
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2330
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 2.067e0

DP
type: SiteQuality
SIO_000300: 3.273772e6

VQSLOD
type: SiteQuality
SIO_000300: -2.479e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.53e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.75e1
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GenotypeQuality
all individuals: 3885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44475
bin: 9.75e1
variant carriers: 527

Latino
type: Population
allele count: 89
allele frequency: 7.686992572119537e-3
allele num: 11578
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 31
allele frequency: 1.878104931540046e-3
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 80
allele frequency: 1.24223602484472e-2
allele num: 6440
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.567928730512249e-3
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 269
allele frequency: 3.109826589595376e-2
allele num: 8650
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 58
allele frequency: 8.704787633198259e-4
allele num: 66630
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.157e1

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 3.281629e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.799e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1998
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variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
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GenotypeQuality
all individuals: 3885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44475
bin: 9.75e1
variant carriers: 66

GenotypeQuality
all individuals: 2044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.924187030979411e-4
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.105590062111801e-4
allele num: 6440
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 9.155035269398169e-4
allele num: 66630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.281629e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.799e0

QD
type: SiteQuality
SIO_000300: 1.157e1

GenotypeQuality
all individuals: 2353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 3952
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variant carriers: 0

GenotypeQuality
all individuals: 2087
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 44482
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 67
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GenotypeQuality
all individuals: 1444
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.506e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.859e0

DP
type: SiteQuality
SIO_000300: 3.277556e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.839e1

VQSLOD
type: SiteQuality
SIO_000300: -3.32e0

QD
type: SiteQuality
SIO_000300: 1.091e1

GenotypeQuality
all individuals: 44447
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.028467595396729e-4
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.255e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 3.27832e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

FS
type: SiteQuality
SIO_000300: 1.977e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.189e0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2189
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1555
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 44447
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 9
allele frequency: 8.660508083140878e-4
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001110410852015e-5
allele num: 66642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.977e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.189e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 3.27832e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 44471
bin: 9.75e1
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GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 1561
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GenotypeQuality
all individuals: 2193
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variant carriers: 0

GenotypeQuality
all individuals: 3988
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variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 7.081e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.87e-1

DP
type: SiteQuality
SIO_000300: 3.278698e6

QD
type: SiteQuality
SIO_000300: 1.621e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
all individuals: 127
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 1523
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GenotypeQuality
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GenotypeQuality
all individuals: 44347
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 2301
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GenotypeQuality
all individuals: 2010
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GenotypeQuality
all individuals: 2173
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.024e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

DP
type: SiteQuality
SIO_000300: 3.280558e6

QD
type: SiteQuality
SIO_000300: 7.35e0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44623
bin: 9.75e1
variant carriers: 1106

GenotypeQuality
all individuals: 2028
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 63
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3960
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 987
allele frequency: 9.497690531177828e-2
allele num: 10392
num of homozygotes: 47

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

Latino
type: Population
allele count: 82
allele frequency: 7.083621285418107e-3
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 8.102268635217861e-4
allele num: 66648
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.514784294716432e-3
allele num: 16504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.26e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.567e1

MQ
type: SiteQuality
SIO_000300: 5.837e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

DP
type: SiteQuality
SIO_000300: 3.288915e6

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44336
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
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variant carriers: 0

GenotypeQuality
all individuals: 3992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.482e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

DP
type: SiteQuality
SIO_000300: 3.273556e6

VQSLOD
type: SiteQuality
SIO_000300: -1.708e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

QD
type: SiteQuality
SIO_000300: 5.29e0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44311
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variant carriers: 16

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2207
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 3884
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.25123818099955e-4
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

DP
type: SiteQuality
SIO_000300: 3.276208e6

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43304
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516990291262136e-5
allele num: 65920
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.573e2

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 3.291856e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.288e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 1.8294e2

QD
type: SiteQuality
SIO_000300: 3.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.005e0

GenotypeQuality
all individuals: 1915
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
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variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.291856e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.005e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 1.8294e2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.573e2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 3.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.288e0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 1541
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 0
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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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1486
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 2135
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variant carriers: 0

GenotypeQuality
all individuals: 4026
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 7.75e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999310158663508e-5
allele num: 66682
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 2.241e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 3.284398e6

FS
type: SiteQuality
SIO_000300: 5.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.981e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.695e0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2347
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 2137
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variant carriers: 0

GenotypeQuality
all individuals: 2051
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2229
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GenotypeQuality
all individuals: 4030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 1543
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1488
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44756
bin: 9.75e1
variant carriers: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
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: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 3.243e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

DP
type: SiteQuality
SIO_000300: 3.284477e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: -6.398e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 2049
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 44759
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.849173739615512e-4
allele num: 66686
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e0

DP
type: SiteQuality
SIO_000300: 3.285251e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 5.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.724e0

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

GenotypeQuality
all individuals: 4074
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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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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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66712
num of homozygotes: 0

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

VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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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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Other
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East Asian
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allele num: 8654
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European (Non-Finnish)
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allele frequency: 1.498890820792613e-5
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num of homozygotes: 0

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

Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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DP
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MQ
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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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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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Other
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South Asian
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East Asian
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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South Asian
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MQ
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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FS
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.89e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.16e-1

FS
type: SiteQuality
SIO_000300: 1.722e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.589e1

DP
type: SiteQuality
SIO_000300: 3.285695e6

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

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44751
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2356
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993407252022775e-5
allele num: 66740
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.722e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.16e-1

DP
type: SiteQuality
SIO_000300: 3.285695e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.589e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.89e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2047
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0