21-43281901-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43281901
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43281901
    reference: chr 21
allele count: 1
allele frequency: 8.765010079761592e-6
allele num: 114090
alternate allele: G
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.703-41A>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.703-41A>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.-9-1420A>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.-9-1420A>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.103-1420A>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.-9-1420A>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.103-1420A>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.103-1420A>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8466
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7384
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/21-43281912-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43281912
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43281912
    reference: chr 21
allele count: 13
allele frequency: 1.156995372018512e-4
allele num: 112360
alternate allele: A
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.-9-1431G>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.-9-1431G>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.103-1431G>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.-9-1431G>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.703-52G>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.103-1431G>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.703-52G>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.103-1431G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16048
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12714
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7198
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

21-43281983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43281983
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43281983
    reference: chr 21
allele count: 1
allele frequency: 9.004466215242761e-6
allele num: 111056
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.-9-1502C>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.-9-1502C>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.702+51C>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.103-1502C>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.103-1502C>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.103-1502C>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.702+51C>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.-10+1361C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5834
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/21-43281987-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43281987
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43281987
    reference: chr 21
allele count: 6
allele frequency: 5.395004226086644e-5
allele num: 111214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-1506T>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.-10+1357T>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.103-1506T>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.702+47T>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.103-1506T>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.702+47T>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.-9-1506T>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.-9-1506T>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13292
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14080
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12937
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5672
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2800
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/21-43281995-CCCAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43281995
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43281991
    reference: chr 21
allele count: 1
allele frequency: 8.973599669771532e-6
allele num: 111438
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.702+35_702+38delTTGG
  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.103-1518_103-1515delTTGG
  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.-10+1345_-10+1348delTTGG
  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.103-1518_103-1515delTTGG
  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.-9-1518_-9-1515delTTGG
  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.-9-1518_-9-1515delTTGG
  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.103-1518_103-1515delTTGG
  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.702+35_702+38delTTGG
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5736
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: CCCAA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

21-43281998-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43281998
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43281998
    reference: chr 21
allele count: 16
allele frequency: 1.429260536330016e-4
allele num: 111946
alternate allele: T
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.-9-1517T>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.-9-1517T>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.103-1517T>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.702+36T>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.-10+1346T>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.702+36T>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.103-1517T>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.103-1517T>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9688
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22568
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1836
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2489
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/21-43282001-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282001
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282001
    reference: chr 21
allele count: 1
allele frequency: 8.908209806157355e-6
allele num: 112256
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.103-1520T>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.-9-1520T>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.103-1520T>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.103-1520T>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.-10+1343T>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.702+33T>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.702+33T>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.-9-1520T>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

21-43282009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282009
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282009
    reference: chr 21
allele count: 1
allele frequency: 8.831269759966088e-6
allele num: 113234
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.702+25C>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.103-1528C>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.103-1528C>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.-9-1528C>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.702+25C>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.-10+1335C>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.-9-1528C>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.103-1528C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29850
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1295
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

21-43282009-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282009
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282009
    reference: chr 21
allele count: 1
allele frequency: 8.831269759966088e-6
allele num: 113234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.103-1528C>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.103-1528C>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.103-1528C>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.702+25C>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.-9-1528C>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.-9-1528C>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.702+25C>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.-10+1335C>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2478
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

21-43282024-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282024
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282024
    reference: chr 21
allele count: 1
allele frequency: 8.639308855291577e-6
allele num: 115750
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.103-1543C>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.-9-1543C>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.702+10C>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.103-1543C>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.-9-1543C>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.103-1543C>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.702+10C>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.-10+1320C>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/21-43282027-AACAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282027
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282023
    reference: chr 21
allele count: 1
allele frequency: 8.615639108109039e-6
allele num: 116068
alternate allele: A
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.702+3_702+6delGTGT
  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.-10+1313_-10+1316delGTGT
  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.-9-1550_-9-1547delGTGT
  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.103-1550_103-1547delGTGT
  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.103-1550_103-1547delGTGT
  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.103-1550_103-1547delGTGT
  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.702+3_702+6delGTGT
  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.-9-1550_-9-1547delGTGT
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.75e1
  variant carriers: 0
hgvs: c.702+3_702+6delGTGT
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: AACAC
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

21-43282035-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282035
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282035
    reference: chr 21
allele count: 4
allele frequency: 3.432887058015791e-5
allele num: 116520
alternate allele: G
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.701A>C
  hgvsp: ENSP00000415471.1:p.Asn234Thr
  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.-10+1309A>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.103-1554A>C
  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.701A>C
  hgvsp: ENSP00000269844.3:p.Asn234Thr
  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.103-1554A>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.103-1554A>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.-9-1554A>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.-9-1554A>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35320
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2478
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3096
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn234Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

21-43282039-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282039
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282039
    reference: chr 21
allele count: 2
allele frequency: 1.715295288083844e-5
allele num: 116598
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.697G>A
  hgvsp: ENSP00000269844.3:p.Val233Met
  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.103-1558G>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.-9-1558G>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.697G>A
  hgvsp: ENSP00000415471.1:p.Val233Met
  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.-9-1558G>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.103-1558G>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.-10+1305G>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.103-1558G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val233Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

21-43282040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282040
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282040
    reference: chr 21
allele count: 4
allele frequency: 3.429355281207133e-5
allele num: 116640
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.-9-1559C>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.103-1559C>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.103-1559C>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.696C>T
  hgvsp: ENST00000433067.1:c.696C>T(p.%3D)
  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.-10+1304C>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.696C>T
  hgvsp: ENST00000269844.3:c.696C>T(p.%3D)
  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.103-1559C>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.-9-1559C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn232Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

21-43282050-A-ATC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282050
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282052
    reference: chr 21
allele count: 1
allele frequency: 8.568099252861745e-6
allele num: 116712
alternate allele: ATC
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.-10+1292_-10+1293dupGA
  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.-9-1571_-9-1570dupGA
  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.684_685dupGA
  hgvsp: ENSP00000269844.3:p.Ile229ArgfsTer4
  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.103-1571_103-1570dupGA
  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.103-1571_103-1570dupGA
  variant of: http://identifiers.org/hgnc/13999
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.684_685dupGA
  hgvsp: ENSP00000415471.1:p.Ile229ArgfsTer4
  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.-9-1571_-9-1570dupGA
  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.103-1571_103-1570dupGA
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3195
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile229ArgfsTer4
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

21-43282054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282054
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282054
    reference: chr 21
allele count: 3
allele frequency: 2.573737581716168e-5
allele num: 116562
alternate allele: T
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.-9-1573G>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.103-1573G>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.-10+1290G>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.103-1573G>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.-9-1573G>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.682G>A
  hgvsp: ENSP00000415471.1:p.Glu228Lys
  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.103-1573G>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.682G>A
  hgvsp: ENSP00000269844.3:p.Glu228Lys
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu228Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

21-43282055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282055
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282055
    reference: chr 21
allele count: 1
allele frequency: 8.580892069539549e-6
allele num: 116538
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.103-1574C>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.-9-1574C>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.681C>T
  hgvsp: ENST00000269844.3:c.681C>T(p.%3D)
  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.103-1574C>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.-10+1289C>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.103-1574C>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.-9-1574C>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.681C>T
  hgvsp: ENST00000433067.1:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42811
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His227His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

21-43282058-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282058
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282058
    reference: chr 21
allele count: 7
allele frequency: 6.015916395950429e-5
allele num: 116358
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.-9-1577G>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.103-1577G>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.-9-1577G>A
  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.678G>A
  hgvsp: ENST00000269844.3:c.678G>A(p.%3D)
  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.103-1577G>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.678G>A
  hgvsp: ENST00000433067.1:c.678G>A(p.%3D)
  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.103-1577G>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.-10+1286G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13931
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro226Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

21-43282067-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282067
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282067
    reference: chr 21
allele count: 2
allele frequency: 1.729116594331956e-5
allele num: 115666
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.669G>C
  hgvsp: ENSP00000415471.1:p.Leu223Phe
  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.103-1586G>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.-10+1277G>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.-9-1586G>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.103-1586G>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.103-1586G>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.669G>C
  hgvsp: ENSP00000269844.3:p.Leu223Phe
  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.-9-1586G>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42498
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu223Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

21-43282075-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282075
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282075
    reference: chr 21
allele count: 4
allele frequency: 3.502197629012205e-5
allele num: 114214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.-9-1594T>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.-9-1594T>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.103-1594T>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.661T>C
  hgvsp: ENSP00000415471.1:p.Ser221Pro
  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.-10+1269T>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.103-1594T>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.661T>C
  hgvsp: ENSP00000269844.3:p.Ser221Pro
  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.103-1594T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30989
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser221Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/21-43282076-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282076
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282076
    reference: chr 21
allele count: 1
allele frequency: 8.756414073308699e-6
allele num: 114202
alternate allele: A
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.-10+1268G>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.660G>T
  hgvsp: ENSP00000415471.1:p.Glu220Asp
  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.103-1595G>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.103-1595G>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.-9-1595G>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.103-1595G>T
  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.660G>T
  hgvsp: ENSP00000269844.3:p.Glu220Asp
  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.-9-1595G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1328
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu220Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/21-43282079-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282079
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282079
    reference: chr 21
allele count: 2
allele frequency: 1.76385508166649e-5
allele num: 113388
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.103-1598T>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.-9-1598T>G
  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.657T>G
  hgvsp: ENST00000433067.1:c.657T>G(p.%3D)
  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.103-1598T>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.-10+1265T>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.103-1598T>G
  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.657T>G
  hgvsp: ENST00000269844.3:c.657T>G(p.%3D)
  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.-9-1598T>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29815
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr219Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

21-43282086-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282086
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282086
    reference: chr 21
allele count: 39
allele frequency: 3.513007134106795e-4
allele num: 111016
alternate allele: A
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.-10+1258A>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.650A>T
  hgvsp: ENSP00000415471.1:p.Tyr217Phe
  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.103-1605A>T
  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.650A>T
  hgvsp: ENSP00000269844.3:p.Tyr217Phe
  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.-9-1605A>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.103-1605A>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.103-1605A>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.-9-1605A>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13049
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26863
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35118
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 9.75e1
  variant carriers: 37
hgvs: p.Tyr217Phe
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

21-43282090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282090
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282090
    reference: chr 21
allele count: 18
allele frequency: 1.648593200468933e-4
allele num: 109184
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.646G>A
  hgvsp: ENSP00000269844.3:p.Gly216Ser
  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.646G>A
  hgvsp: ENSP00000415471.1:p.Gly216Ser
  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.-10+1254G>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.103-1609G>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.-9-1609G>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.103-1609G>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.103-1609G>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.-9-1609G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24928
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12488
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly216Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

21-43282091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282091
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282091
    reference: chr 21
allele count: 7
allele frequency: 6.431813587665619e-5
allele num: 108834
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.645C>T
  hgvsp: ENST00000269844.3:c.645C>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.645C>T
  hgvsp: ENST00000433067.1:c.645C>T(p.%3D)
  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.103-1610C>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.103-1610C>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.103-1610C>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.-9-1610C>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.-10+1253C>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.-9-1610C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24705
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12545
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys215Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

21-43282096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282096
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282096
    reference: chr 21
allele count: 1
allele frequency: 9.328010148875041e-6
allele num: 107204
alternate allele: T
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.-9-1615G>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.-9-1615G>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.640G>A
  hgvsp: ENSP00000415471.1:p.Glu214Lys
  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.103-1615G>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.103-1615G>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.103-1615G>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.-10+1248G>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.640G>A
  hgvsp: ENSP00000269844.3:p.Glu214Lys
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu214Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

21-43282097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282097
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282097
    reference: chr 21
allele count: 11
allele frequency: 1.033620867865667e-4
allele num: 106422
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.103-1616C>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.103-1616C>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.-10+1247C>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.-9-1616C>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.-9-1616C>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.639C>T
  hgvsp: ENST00000269844.3:c.639C>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.639C>T
  hgvsp: ENST00000433067.1:c.639C>T(p.%3D)
  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.103-1616C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22528
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11455
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala213Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

21-43282097-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282097
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282097
    reference: chr 21
allele count: 1
allele frequency: 9.396553344233335e-6
allele num: 106422
alternate allele: T
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.103-1616C>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.103-1616C>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.-10+1247C>A
  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.639C>A
  hgvsp: ENST00000269844.3:c.639C>A(p.%3D)
  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.-9-1616C>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.639C>A
  hgvsp: ENST00000433067.1:c.639C>A(p.%3D)
  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.103-1616C>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.-9-1616C>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala213Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

21-43282103-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282103
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282103
    reference: chr 21
allele count: 38
allele frequency: 3.633720930232558e-4
allele num: 104576
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.-9-1622C>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.-9-1622C>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.103-1622C>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.103-1622C>G
  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.633C>G
  hgvsp: ENST00000269844.3:c.633C>G(p.%3D)
  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.103-1622C>G
  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.633C>G
  hgvsp: ENST00000433067.1:c.633C>G(p.%3D)
  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.-10+1241C>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10867
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10367
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 20926
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 9.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26773
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly211Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

21-43282108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282108
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282108
    reference: chr 21
allele count: 28
allele frequency: 2.721776153352645e-4
allele num: 102874
alternate allele: T
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.-9-1627G>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.628G>A
  hgvsp: ENSP00000415471.1:p.Ala210Thr
  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.103-1627G>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.-10+1236G>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.103-1627G>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.-9-1627G>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.628G>A
  hgvsp: ENSP00000269844.3:p.Ala210Thr
  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.103-1627G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11471
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19316
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 8.25e1
  variant carriers: 1
hgvs: p.Ala210Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

21-43282109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282109
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282109
    reference: chr 21
allele count: 1
allele frequency: 9.755907201810697e-6
allele num: 102502
alternate allele: T
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.103-1628G>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.103-1628G>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.-9-1628G>A
  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.627G>A
  hgvsp: ENST00000269844.3:c.627G>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.627G>A
  hgvsp: ENST00000433067.1:c.627G>A(p.%3D)
  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.-9-1628G>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.-10+1235G>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.103-1628G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18788
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly209Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

21-43282120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282120
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282120
    reference: chr 21
allele count: 1
allele frequency: 1.023101634916413e-5
allele num: 97742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.103-1639A>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.-9-1639A>G
  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.620-4A>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.-9-1639A>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.103-1639A>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.-10+1224A>G
  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.620-4A>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.103-1639A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13225
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19469
  bin: 6.25e1
  variant carriers: 0
hgvs: c.620-4A>G
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/21-43282130-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282130
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282130
    reference: chr 21
allele count: 1
allele frequency: 1.103630945811721e-5
allele num: 90610
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.-9-1649G>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.103-1649G>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.-9-1649G>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.103-1649G>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.-10+1214G>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.620-14G>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.620-14G>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.103-1649G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25549
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4753
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

21-43282134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282134
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282134
    reference: chr 21
allele count: 1
allele frequency: 1.156925355176084e-5
allele num: 86436
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.103-1653C>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.620-18C>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.103-1653C>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.620-18C>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.-10+1210C>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.-9-1653C>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.103-1653C>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.-9-1653C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2482
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

21-43282136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282136
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282136
    reference: chr 21
allele count: 34
allele frequency: 3.949722357751911e-4
allele num: 86082
alternate allele: T
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.103-1655G>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.103-1655G>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.-10+1208G>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.-9-1655G>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.620-20G>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.103-1655G>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.-9-1655G>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.620-20G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22151
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14766
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5219
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7947
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

21-43282137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282137
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282137
    reference: chr 21
allele count: 1
allele frequency: 1.189598153743665e-5
allele num: 84062
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.-9-1656C>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.103-1656C>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.103-1656C>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.-9-1656C>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.620-21C>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.103-1656C>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.620-21C>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.-10+1207C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2793
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

21-43282142-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282142
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282142
    reference: chr 21
allele count: 1
allele frequency: 1.21129899704443e-5
allele num: 82556
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.620-26A>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.-9-1661A>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.-10+1202A>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.103-1661A>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.-9-1661A>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.620-26A>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.103-1661A>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.103-1661A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

21-43282144-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282144
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282144
    reference: chr 21
allele count: 4
allele frequency: 4.898119122257053e-5
allele num: 81664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-1663C>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.103-1663C>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.103-1663C>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.620-28C>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.-9-1663C>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.-9-1663C>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.620-28C>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.-10+1200C>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22054
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3628
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5598
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

21-43282152-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282152
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282152
    reference: chr 21
allele count: 2
allele frequency: 2.589197866500958e-5
allele num: 77244
alternate allele: A
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.-10+1192A>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.103-1671A>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.-9-1671A>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.103-1671A>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.103-1671A>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.620-36A>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.-9-1671A>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.620-36A>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20573
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2824
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5797
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/21-43282153-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282153
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282153
    reference: chr 21
allele count: 0
allele frequency: 0.0e0
allele num: 76404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-1672G>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.-9-1672G>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.620-37G>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.103-1672G>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.-10+1191G>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.103-1672G>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.620-37G>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.-9-1672G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18103
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22652
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2764
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

21-43282155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282155
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282155
    reference: chr 21
allele count: 104
allele frequency: 1.382721301885287e-3
allele num: 75214
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.620-39C>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.-10+1189C>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.103-1674C>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.103-1674C>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.-9-1674C>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.103-1674C>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.-9-1674C>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.620-39C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19842
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 18586
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21664
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 9.75e1
  variant carriers: 101
genotype quality: GenotypeQuality
  all individuals: 3927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5782
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 9.25e1
  variant carriers: 7
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

21-43282160-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282160
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282160
    reference: chr 21
allele count: 1
allele frequency: 1.382666887893369e-5
allele num: 72324
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.-10+1184C>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.-9-1679C>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.103-1679C>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.620-44C>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.103-1679C>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.-9-1679C>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.620-44C>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.103-1679C>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18658
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5355
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19555
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1480
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

21-43282167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43282167
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43282167
    reference: chr 21
allele count: 11
allele frequency: 1.622706083672626e-4
allele num: 67788
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.103-1686G>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.620-51G>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.-9-1686G>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.103-1686G>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.620-51G>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.103-1686G>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.-9-1686G>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.-10+1177G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21252
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17469
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4888
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

21-43287358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287358
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287358
    reference: chr 21
allele count: 34
allele frequency: 2.877064717032223e-4
allele num: 118176
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.619+51G>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.103-6877G>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.-9-6877G>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.103-6877G>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.619+51G>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.-9-6877G>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.103-6877G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-43287359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287359
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287359
    reference: chr 21
allele count: 26
allele frequency: 2.198248165308262e-4
allele num: 118276
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.103-6878C>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.103-6878C>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.-9-6878C>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.619+50C>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.619+50C>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.-9-6878C>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.103-6878C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3858
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3676
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

21-43287359-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287359
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287359
    reference: chr 21
allele count: 1
allele frequency: 8.454800635801008e-6
allele num: 118276
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.619+50C>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.-9-6878C>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.619+50C>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.103-6878C>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.-9-6878C>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.103-6878C>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.103-6878C>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27255
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

21-43287359-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287359
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287360
    reference: chr 21
allele count: 1
allele frequency: 8.454800635801008e-6
allele num: 118276
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.619+49dupA
  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.-9-6879dupA
  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.103-6879dupA
  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.103-6879dupA
  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.-9-6879dupA
  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.619+49dupA
  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.103-6879dupA
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3858
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3676
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

21-43287365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287365
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287365
    reference: chr 21
allele count: 5
allele frequency: 4.228830474643933e-5
allele num: 118236
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.103-6884G>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.103-6884G>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.619+44G>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.-9-6884G>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.619+44G>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.103-6884G>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.-9-6884G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27243
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4074
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

21-43287370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287370
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287370
    reference: chr 21
allele count: 1
allele frequency: 8.446088616361763e-6
allele num: 118398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-6889T>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.619+39T>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.619+39T>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.103-6889T>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.103-6889T>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.-9-6889T>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.-9-6889T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8902
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

21-43287371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287371
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287371
    reference: chr 21
allele count: 1
allele frequency: 8.443806467955754e-6
allele num: 118430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-6890C>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.-9-6890C>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.619+38C>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.103-6890C>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.103-6890C>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.-9-6890C>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.619+38C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4113
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/21-43287377-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287377
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287377
    reference: chr 21
allele count: 1
allele frequency: 8.435970980259829e-6
allele num: 118540
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000408592
  ensembl transcript: ENST00000422911
  gene symbol: PRDM15
  hgvsc: ENST00000422911.1:c.103-6896T>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.619+32T>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.-9-6896T>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.103-6896T>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.103-6896T>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.619+32T>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.-9-6896T>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4154
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27238
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9653
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

21-43287380-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287380
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287379
    reference: chr 21
allele count: 1
allele frequency: 8.427865895797866e-6
allele num: 118654
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.619+28delA
  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.103-6900delA
  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.619+28delA
  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.-9-6900delA
  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.103-6900delA
  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.103-6900delA
  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.-9-6900delA
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4174
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27238
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: AT
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

21-43287386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287386
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287386
    reference: chr 21
allele count: 1
allele frequency: 8.412409987213136e-6
allele num: 118872
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.103-6905G>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.619+23G>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.-9-6905G>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.-9-6905G>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.103-6905G>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.619+23G>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.103-6905G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10410
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD

21-43287395-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287395
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287395
    reference: chr 21
allele count: 2
allele frequency: 1.676558360996546e-5
allele num: 119292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000444044
  ensembl transcript: ENST00000538201
  gene symbol: PRDM15
  hgvsc: ENST00000538201.1:c.-9-6914T>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.-9-6914T>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.103-6914T>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.103-6914T>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.103-6914T>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.619+14T>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.619+14T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4271
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3864
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

21-43287415-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287415
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287415
    reference: chr 21
allele count: 2
allele frequency: 1.666972278251013e-5
allele num: 119978
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.103-6934G>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.-9-6934G>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.613G>A
  hgvsp: ENSP00000269844.3:p.Gly205Arg
  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.-9-6934G>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.613G>A
  hgvsp: ENSP00000415471.1:p.Gly205Arg
  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.103-6934G>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.103-6934G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27236
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly205Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

21-43287416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287416
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287416
    reference: chr 21
allele count: 3
allele frequency: 2.499916669444352e-5
allele num: 120004
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.103-6935C>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.103-6935C>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.612C>T
  hgvsp: ENST00000433067.1:c.612C>T(p.%3D)
  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.-9-6935C>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.612C>T
  hgvsp: ENST00000269844.3:c.612C>T(p.%3D)
  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.103-6935C>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.-9-6935C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3866
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27235
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12307
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn204Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

21-43287419-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287419
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287419
    reference: chr 21
allele count: 20
allele frequency: 1.666083537428567e-4
allele num: 120042
alternate allele: T
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.609G>A
  hgvsp: ENST00000433067.1:c.609G>A(p.%3D)
  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.-9-6938G>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.103-6938G>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.103-6938G>A
  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.609G>A
  hgvsp: ENST00000269844.3:c.609G>A(p.%3D)
  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.-9-6938G>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.103-6938G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7850
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4366
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala203Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

21-43287420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287420
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287420
    reference: chr 21
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.608C>T
  hgvsp: ENSP00000269844.3:p.Ala203Val
  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.103-6939C>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.-9-6939C>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.103-6939C>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.103-6939C>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.608C>T
  hgvsp: ENSP00000415471.1:p.Ala203Val
  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.-9-6939C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3968
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27226
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala203Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

21-43287420-GCAATCTTCCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287420
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287410
    reference: chr 21
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  variant of: http://identifiers.org/hgnc/13999
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000415471
  ensembl transcript: ENST00000433067
  gene symbol: PRDM15
  hgvsp: ENSP00000415471.1:p.Gly200ArgfsTer22
  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
  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
  hgvsp: ENSP00000269844.3:p.Gly200ArgfsTer22
  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
  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
  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
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3968
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27226
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly200ArgfsTer22
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: GCAATCTTCCC
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/21-43287421-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287421
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287421
    reference: chr 21
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.607G>T
  hgvsp: ENSP00000269844.3:p.Ala203Ser
  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.103-6940G>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.607G>T
  hgvsp: ENSP00000415471.1:p.Ala203Ser
  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.103-6940G>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.-9-6940G>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.103-6940G>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.-9-6940G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4373
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala203Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

21-43287422-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287422
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287422
    reference: chr 21
allele count: 5
allele frequency: 4.16382138871771e-5
allele num: 120082
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.103-6941T>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.-9-6941T>A
  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.606T>A
  hgvsp: ENST00000269844.3:c.606T>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.606T>A
  hgvsp: ENST00000433067.1:c.606T>A(p.%3D)
  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.103-6941T>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.103-6941T>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.-9-6941T>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27226
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile202Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-43287423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287423
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287423
    reference: chr 21
allele count: 9
allele frequency: 7.494254404956201e-5
allele num: 120092
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.605T>C
  hgvsp: ENSP00000415471.1:p.Ile202Thr
  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.-9-6942T>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.103-6942T>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.605T>C
  hgvsp: ENSP00000269844.3:p.Ile202Thr
  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.-9-6942T>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.103-6942T>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.103-6942T>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile202Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/21-43287436-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287436
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287436
    reference: chr 21
allele count: 1
allele frequency: 8.320990530712775e-6
allele num: 120178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-6955G>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.-9-6955G>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.592G>T
  hgvsp: ENSP00000415471.1:p.Ala198Ser
  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.-9-6955G>T
  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.592G>T
  hgvsp: ENSP00000269844.3:p.Ala198Ser
  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.103-6955G>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.103-6955G>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala198Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

21-43287437-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287437
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287436
    reference: chr 21
allele count: 1
allele frequency: 8.320298199487469e-6
allele num: 120188
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.103-6957delC
  variant of: http://identifiers.org/hgnc/13999
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.590delC
  hgvsp: ENSP00000415471.1:p.Pro197GlnfsTer28
  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.590delC
  hgvsp: ENSP00000269844.3:p.Pro197GlnfsTer28
  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.103-6957delC
  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.-9-6957delC
  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.-9-6957delC
  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.103-6957delC
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7380
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro197GlnfsTer28
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: TG
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

21-43287451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287451
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287451
    reference: chr 21
allele count: 2
allele frequency: 1.664281196951037e-5
allele num: 120172
alternate allele: T
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.-9-6970G>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.577G>A
  hgvsp: ENSP00000415471.1:p.Glu193Lys
  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.103-6970G>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.-9-6970G>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.103-6970G>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.577G>A
  hgvsp: ENSP00000269844.3:p.Glu193Lys
  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.103-6970G>A
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu193Lys
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

21-43287457-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287457
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287457
    reference: chr 21
allele count: 1
allele frequency: 8.320852055250457e-6
allele num: 120180
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.571A>G
  hgvsp: ENSP00000415471.1:p.Asn191Asp
  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.-9-6976A>G
  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.571A>G
  hgvsp: ENSP00000269844.3:p.Asn191Asp
  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.103-6976A>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.-9-6976A>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.103-6976A>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.103-6976A>G
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4356
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12426
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn191Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

21-43287457-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287457
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287456
    reference: chr 21
allele count: 56
allele frequency: 4.659677150940256e-4
allele num: 120180
alternate allele: T
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.-9-6977delG
  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.103-6977delG
  variant of: http://identifiers.org/hgnc/13999
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.570delG
  hgvsp: ENSP00000415471.1:p.Asn191ThrfsTer34
  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.103-6977delG
  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.-9-6977delG
  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.570delG
  hgvsp: ENSP00000269844.3:p.Asn191ThrfsTer34
  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.103-6977delG
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3866
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3695
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn191ThrfsTer34
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: TC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

21-43287462-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287462
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287462
    reference: chr 21
allele count: 1
allele frequency: 8.321959988016378e-6
allele num: 120164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000381556
  ensembl transcript: ENST00000398548
  gene symbol: PRDM15
  hgvsc: ENST00000398548.1:c.103-6981G>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.103-6981G>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.566G>C
  hgvsp: ENSP00000415471.1:p.Trp189Ser
  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.566G>C
  hgvsp: ENSP00000269844.3:p.Trp189Ser
  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.-9-6981G>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.-9-6981G>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.103-6981G>C
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Trp189Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

21-43287464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287464
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287464
    reference: chr 21
allele count: 3
allele frequency: 2.496754219514631e-5
allele num: 120156
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141956
  ensembl protein: ENSP00000269844
  ensembl transcript: ENST00000269844
  gene symbol: PRDM15
  hgvsc: ENST00000269844.3:c.564C>T
  hgvsp: ENST00000269844.3:c.564C>T(p.%3D)
  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.103-6983C>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.103-6983C>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.-9-6983C>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.564C>T
  hgvsp: ENST00000433067.1:c.564C>T(p.%3D)
  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.-9-6983C>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.103-6983C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4367
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser188Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

21-43287470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287470
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287470
    reference: chr 21
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: A
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.558C>T
  hgvsp: ENST00000433067.1:c.558C>T(p.%3D)
  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.-9-6989C>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.103-6989C>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.558C>T
  hgvsp: ENST00000269844.3:c.558C>T(p.%3D)
  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.-9-6989C>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.103-6989C>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.103-6989C>T
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27187
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn186Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

21-43287470-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43287470
    reference: chr 21
  end: Position
    type: ExactPosition
    position: 43287470
    reference: chr 21
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
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.-9-6989C>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.558C>G
  hgvsp: ENSP00000415471.1:p.Asn186Lys
  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.103-6989C>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.103-6989C>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.103-6989C>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.-9-6989C>G
  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.558C>G
  hgvsp: ENSP00000269844.3:p.Asn186Lys
  variant of: http://identifiers.org/hgnc/13999
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12345
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn186Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G

GenotypeQuality
all individuals: 4211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7047
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3916
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12145
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.351037965214139e-5
allele num: 10694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

QD
type: SiteQuality
SIO_000300: 1.737e1

DP
type: SiteQuality
SIO_000300: 1.344727e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 1.0651e1

VQSLOD
type: SiteQuality
SIO_000300: -3.725e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.862e1

GenotypeQuality
all individuals: 388
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10484
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 13
allele frequency: 2.090301003344482e-4
allele num: 62192
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.347e1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 1.327601e6

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.642467643387425e-5
allele num: 60884
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10430
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15046
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.835098187063568e-5
allele num: 61006
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 1.218e1

FS
type: SiteQuality
SIO_000300: 3.184e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

InbreedingCoeff
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SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.240122e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15054
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.635643953024306e-5
allele num: 61138
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

DP
type: SiteQuality
SIO_000300: 1.282192e6

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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variant carriers: 0

European (Finnish)
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allele count: 13
allele frequency: 2.114508783344177e-3
allele num: 6148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.882176799895847e-5
allele num: 61448
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.7e-1

VQSLOD
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.357e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.622112639501687e-5
allele num: 61648
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 848
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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FS
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 10636
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 62288
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European (Finnish)
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East Asian
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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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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East Asian
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num of homozygotes: 0

African
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Other
type: Population
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 62288
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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Latino
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FS
type: SiteQuality
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6290
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Other
type: Population
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Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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num of homozygotes: 0

FS
type: SiteQuality
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42655
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63996
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.585791309863622e-4
allele num: 6306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.115e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.73e0

QD
type: SiteQuality
SIO_000300: 2.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

DP
type: SiteQuality
SIO_000300: 1.460995e6

MQ
type: SiteQuality
SIO_000300: 5.805e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.221420350265965e-5
allele num: 64294
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

FS
type: SiteQuality
SIO_000300: 6.850000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.471083e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.108776074859328e-5
allele num: 64334
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.048e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.35e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.505e0

DP
type: SiteQuality
SIO_000300: 1.474379e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.553277415346381e-5
allele num: 64380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.010234798314269e-4
allele num: 9966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15516
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.198e1

FS
type: SiteQuality
SIO_000300: 4.112e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.476392e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

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
all individuals: 883
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.002606777621817e-4
allele num: 9974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11052
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.652e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-1

QD
type: SiteQuality
SIO_000300: 1.882e1

DP
type: SiteQuality
SIO_000300: 1.477598e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

MQ
type: SiteQuality
SIO_000300: 6.024e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.111e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 694
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GenotypeQuality
all individuals: 1400
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.004016064257028e-4
allele num: 9960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.289656951250967e-4
allele num: 15508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.702e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.478801e6

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

QD
type: SiteQuality
SIO_000300: 1.094e1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.448284756254837e-5
allele num: 15508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
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: 0
allele frequency: 0.0e0
allele num: 64316
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.47876e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.082e0

VQSLOD
type: SiteQuality
SIO_000300: -6.108e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.455e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557535356052582e-5
allele num: 64204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.230808994572241e-4
allele num: 15476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.481511e6

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

QD
type: SiteQuality
SIO_000300: 1.022e1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.823486506199854e-4
allele num: 10968
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63786
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.471206e6

FS
type: SiteQuality
SIO_000300: 1.625e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.424e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.68e-1

GenotypeQuality
all individuals: 403
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variant carriers: 0

GenotypeQuality
all individuals: 36
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10822
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.355258976803305e-5
allele num: 62940
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

MQ
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

DP
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BaseQRankSum
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SIO_000300: 1.4e0

FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6112
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10822
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 62932
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.186239620403321e-4
allele num: 8430
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 2.383222116301239e-4
allele num: 8392
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62396
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Latino
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allele frequency: 0.0e0
allele num: 10738
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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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DP
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SIO_000300: 1.430694e6

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

Other
type: Population
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allele frequency: 1.190476190476191e-3
allele num: 840
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 35
allele frequency: 5.749203324682151e-4
allele num: 60878
num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 5.091649694501018e-4
allele num: 5892
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14950
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8308
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DP
type: SiteQuality
SIO_000300: 1.387302e6

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 1.189e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.049979000419992e-4
allele num: 9524
num of homozygotes: 0

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

East Asian
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allele count: 11
allele frequency: 1.340482573726542e-3
allele num: 8206
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 6
allele frequency: 1.003277372750987e-4
allele num: 59804
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
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MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.715e0

QD
type: SiteQuality
SIO_000300: 1.26e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 2.71333604666938e-4
allele num: 14742
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.035246727089627e-5
allele num: 59580
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African
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Other
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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Other
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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East Asian
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Other
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European (Non-Finnish)
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African
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MQ
type: SiteQuality
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FS
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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Other
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.312499e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
all individuals: 882
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14967
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 805
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.959893423082317e-4
allele num: 57048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.494505494505495e-4
allele num: 5460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.259445843828715e-3
allele num: 794
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

FS
type: SiteQuality
SIO_000300: 2.97e0

DP
type: SiteQuality
SIO_000300: 1.281467e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.351e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e-1

GenotypeQuality
all individuals: 16512
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 9.75e1
variant carriers: 27

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.677806341045416e-4
allele num: 56016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14278
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 9.493670886075949e-4
allele num: 9480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.588673621460507e-4
allele num: 5368
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.094331363536879e-4
allele num: 9138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.256448e6

QD
type: SiteQuality
SIO_000300: 1.251e1

FS
type: SiteQuality
SIO_000300: 1.381e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.415e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1083
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 550
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.790766806346477e-5
allele num: 55842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.279e0

DP
type: SiteQuality
SIO_000300: 1.248824e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

QD
type: SiteQuality
SIO_000300: 7.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 319
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21559
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1328
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.885582833653882e-5
allele num: 53034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5028
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.664e0

MQRankSum
type: SiteQuality
SIO_000300: -7.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

FS
type: SiteQuality
SIO_000300: 6.043e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.512e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 1.162722e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

GenotypeQuality
all individuals: 1027
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1729
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4815
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variant carriers: 0

GenotypeQuality
all individuals: 10277
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.048089132839061e-5
allele num: 48826
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

FS
type: SiteQuality
SIO_000300: 2.158e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.113e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.794e0

QD
type: SiteQuality
SIO_000300: 7.97e0

DP
type: SiteQuality
SIO_000300: 1.029677e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

GenotypeQuality
all individuals: 1020
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25086
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5323
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7495
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.158428663932657e-5
allele num: 46330
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

DP
type: SiteQuality
SIO_000300: 9.8303e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.405999999999999e-1

FS
type: SiteQuality
SIO_000300: 9.206e0

GenotypeQuality
all individuals: 1247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25626
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 1001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.387732445184569e-4
allele num: 7206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6662
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 2.976928801786157e-3
allele num: 8062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4314
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 6.891271056661562e-4
allele num: 13060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

FS
type: SiteQuality
SIO_000300: 2.756e0

DP
type: SiteQuality
SIO_000300: 9.78999e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5006
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.541782300339192e-4
allele num: 6486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.945e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.225e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

FS
type: SiteQuality
SIO_000300: 1.373e0

DP
type: SiteQuality
SIO_000300: 9.70135e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.22e0

GenotypeQuality
all individuals: 256
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2454
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 741
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5635
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.275312855517634e-5
allele num: 43950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12780
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.899e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

DP
type: SiteQuality
SIO_000300: 9.35464e5

QD
type: SiteQuality
SIO_000300: 1.316e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.241e0

VQSLOD
type: SiteQuality
SIO_000300: -7.672e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeQuality
all individuals: 5964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 734
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43380
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 6.30715862503942e-4
allele num: 6342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12702
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.21e-1

QD
type: SiteQuality
SIO_000300: 1.025e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

DP
type: SiteQuality
SIO_000300: 9.29276e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.327e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2452
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 3.236245954692557e-4
allele num: 6180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -5.956e-1

DP
type: SiteQuality
SIO_000300: 8.93787e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

QD
type: SiteQuality
SIO_000300: 8.18e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

GenotypeQuality
all individuals: 5236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4769
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5777
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2854
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.497e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 8.90299e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

QD
type: SiteQuality
SIO_000300: 5.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 383
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variant carriers: 3

GenotypeQuality
all individuals: 3000
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 522
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5013
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 742
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2926
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 8.25e1
variant carriers: 1

Latino
type: Population
allele count: 2
allele frequency: 3.371544167228591e-4
allele num: 5932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.531004808909137e-5
allele num: 39510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

South Asian
type: Population
allele count: 101
allele frequency: 8.220739052580172e-3
allele num: 12286
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5786
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.497e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

DP
type: SiteQuality
SIO_000300: 8.83712e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 3014
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 3765
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4402
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variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
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variant carriers: 0

GenotypeQuality
all individuals: 5747
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.80766449746927e-4
allele num: 5532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12096
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 8.70968e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.783e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.716e1

GenotypeQuality
all individuals: 921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5240
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variant carriers: 0

GenotypeQuality
all individuals: 987
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variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2468
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1323
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 347
bin: 5.75e1
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GenotypeQuality
all individuals: 1288
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
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variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4912
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 8.473140145738011e-4
allele num: 11802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5186
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.446340757882557e-4
allele num: 6914
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.182e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.143e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

DP
type: SiteQuality
SIO_000300: 8.63131e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3961
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27271
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 3855
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 31
allele frequency: 2.700818958006621e-3
allele num: 11478
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.050919852335479e-5
allele num: 65554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15040
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.815469179426777e-5
allele num: 10188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

DP
type: SiteQuality
SIO_000300: 2.532874e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.305e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.17e0

GenotypeQuality
all individuals: 2205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27255
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 1050
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
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variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 6.75e1
variant carriers: 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: 8446
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65574
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.322751322751323e-4
allele num: 15120
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 2.356637863315004e-3
allele num: 10184
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

DP
type: SiteQuality
SIO_000300: 2.531737e6

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3676
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15120
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524994662518681e-5
allele num: 65574
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

QD
type: SiteQuality
SIO_000300: 1.321e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

DP
type: SiteQuality
SIO_000300: 2.531737e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.613756613756614e-5
allele num: 15120
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.531737e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.321e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

GenotypeQuality
all individuals: 73
bin: 2.5e0
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: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1980
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variant carriers: 0

GenotypeQuality
all individuals: 8353
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.309504898067249e-4
allele num: 15108
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.062e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

FS
type: SiteQuality
SIO_000300: 2.126e0

DP
type: SiteQuality
SIO_000300: 2.534006e6

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1983
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variant carriers: 0

GenotypeQuality
all individuals: 3963
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524576167825345e-5
allele num: 65592
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

DP
type: SiteQuality
SIO_000300: 2.537962e6

MQRankSum
type: SiteQuality
SIO_000300: -9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.32e-1

FS
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

QD
type: SiteQuality
SIO_000300: 1.594e1

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 731
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variant carriers: 0

GenotypeQuality
all individuals: 27237
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65604
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.183712121212121e-4
allele num: 8448
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.372e0

QD
type: SiteQuality
SIO_000300: 1.581e1

FS
type: SiteQuality
SIO_000300: 8.69e-1

DP
type: SiteQuality
SIO_000300: 2.538707e6

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
all individuals: 3857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 2206
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variant carriers: 0

GenotypeQuality
all individuals: 3963
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523786304208698e-5
allele num: 65626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

QD
type: SiteQuality
SIO_000300: 1.542e1

VQSLOD
type: SiteQuality
SIO_000300: -2.168e0

DP
type: SiteQuality
SIO_000300: 2.5443e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 4.929e0

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

MQ
type: SiteQuality
SIO_000300: 5.833e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.741e0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 461
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variant carriers: 0

GenotypeQuality
all individuals: 3860
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variant carriers: 0

GenotypeQuality
all individuals: 9975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 2.547922e6

MQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

FS
type: SiteQuality
SIO_000300: 2.542e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15520
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.182592242194891e-4
allele num: 8456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 8.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.118e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.893e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 2.555606e6

FS
type: SiteQuality
SIO_000300: 1.425e0

QD
type: SiteQuality
SIO_000300: 1.486e1

GenotypeQuality
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bin: 9.25e1
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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GenotypeQuality
all individuals: 27238
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65848
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.364625206904706e-4
allele num: 8458
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 2.565848e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.784735812133073e-5
allele num: 10220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.153088850603002e-5
allele num: 16252
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.22e-2

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.412e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

FS
type: SiteQuality
SIO_000300: 4.709e0

DP
type: SiteQuality
SIO_000300: 2.578212e6

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-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
all individuals: 3966
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.147037128104254e-5
allele num: 16268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.027642374882679e-5
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.179801793298726e-4
allele num: 8476
num of homozygotes: 0

African
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allele frequency: 3.915426781519186e-4
allele num: 10216
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 (Finnish)
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allele frequency: 0.0e0
allele num: 6588
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European (Non-Finnish)
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allele count: 15
allele frequency: 2.270113202978388e-4
allele num: 66076
num of homozygotes: 0

South Asian
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num of homozygotes: 0

BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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QD
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.513454611496201e-5
allele num: 66074
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.513454611496201e-5
allele num: 66074
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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DP
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QD
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FS
type: SiteQuality
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MQ
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ClippingRankSum
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SIO_000300: -2.352e0

VQSLOD
type: SiteQuality
SIO_000300: -2.637e-1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51336299524804e-5
allele num: 66078
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.24e1

FS
type: SiteQuality
SIO_000300: 4.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.105e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 2.57876e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

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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variant carriers: 0

South Asian
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allele count: 5
allele frequency: 3.065228052967141e-4
allele num: 16312
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66086
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.94e-1

FS
type: SiteQuality
SIO_000300: 1.116e0

DP
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.361779391738538e-4
allele num: 66090
num of homozygotes: 0

Other
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allele num: 902
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South Asian
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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MQRankSum
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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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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East Asian
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Latino
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Other
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 1.512035805007863e-5
allele num: 66136
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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FS
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QD
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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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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Latino
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Other
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South Asian
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African
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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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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27229
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2024
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3866
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512081531436175e-5
allele num: 66134
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: 6588
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.259e1

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

MQRankSum
type: SiteQuality
SIO_000300: 8.29e-1

MQ
type: SiteQuality
SIO_000300: 6.031e1

FS
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

DP
type: SiteQuality
SIO_000300: 2.580595e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27229
bin: 9.75e1
variant carriers: 55

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12426
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66134
num of homozygotes: 0

African
type: Population
allele count: 55
allele frequency: 5.380551751125024e-3
allele num: 10222
num of homozygotes: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 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: 8480
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

QD
type: SiteQuality
SIO_000300: 1.259e1

MQ
type: SiteQuality
SIO_000300: 6.031e1

FS
type: SiteQuality
SIO_000300: 5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.11e-2

DP
type: SiteQuality
SIO_000300: 2.580595e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

GenotypeQuality
all individuals: 2208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3868
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3966
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27190
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
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: 1.512264464809606e-5
allele num: 66126
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.587e1

DP
type: SiteQuality
SIO_000300: 2.576413e6

MQ
type: SiteQuality
SIO_000300: 5.918e1

FS
type: SiteQuality
SIO_000300: 6.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.508e0

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27190
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2018
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.959247648902821e-4
allele num: 10208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
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: 1.512355948095944e-5
allele num: 66122
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: 8484
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

FS
type: SiteQuality
SIO_000300: 1.254e0

QD
type: SiteQuality
SIO_000300: 1.371e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.576166e6

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3967
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12345
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
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: 66110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.796238244514106e-5
allele num: 10208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.679e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 2.73e0

DP
type: SiteQuality
SIO_000300: 2.575183e6

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3967
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27187
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.119202056051891e-5
allele num: 16342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0