15-74315406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315406
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315406
    reference: chr 15
allele count: 1
allele frequency: 9.314803085062781e-6
allele num: 107356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.840C>T
  hgvsp: ENST00000569965.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.840C>T
  hgvsp: ENST00000569477.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.840C>T
  hgvsp: ENST00000567543.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.840C>T
  hgvsp: ENST00000395135.3:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.840C>T
  hgvsp: ENST00000395132.2:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.691C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.840C>T
  hgvsp: ENST00000563500.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.840C>T
  hgvsp: ENST00000359928.4:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.840C>T
  hgvsp: ENST00000268058.3:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.161C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.840C>T
  hgvsp: ENST00000565898.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.154C>T
  hgvsp: ENST00000565239.1:c.154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.840C>T
  hgvsp: ENST00000436891.3:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.85C>T
  hgvsp: ENST00000567606.1:c.85C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.840C>T
  hgvsp: ENST00000354026.6:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.840C>T
  hgvsp: ENST00000435786.2:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.840C>T
  hgvsp: ENST00000564428.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.840C>T
  hgvsp: ENST00000268059.6:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg280Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

15-74315417-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315417
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315417
    reference: chr 15
allele count: 1
allele frequency: 9.19709371838499e-6
allele num: 108730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.96G>A
  hgvsp: ENSP00000457669.1:p.Arg33His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.851G>A
  hgvsp: ENSP00000315434.8:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.851G>A
  hgvsp: ENSP00000395576.2:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.851G>A
  hgvsp: ENSP00000353004.4:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.165G>A
  hgvsp: ENSP00000456989.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.851G>A
  hgvsp: ENSP00000378567.3:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.851G>A
  hgvsp: ENSP00000378564.2:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.851G>A
  hgvsp: ENSP00000394642.3:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.851G>A
  hgvsp: ENSP00000268058.3:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.851G>A
  hgvsp: ENSP00000455838.1:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.851G>A
  hgvsp: ENSP00000457032.1:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.851G>A
  hgvsp: ENSP00000455612.1:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.851G>A
  hgvsp: ENSP00000457023.1:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.851G>A
  hgvsp: ENSP00000456486.1:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.851G>A
  hgvsp: ENSP00000456277.1:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.851G>A
  hgvsp: ENSP00000268059.6:p.Arg284His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.172G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.702G>A
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg284His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

15-74315421-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315421
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315421
    reference: chr 15
allele count: 1
allele frequency: 9.163551059306502e-6
allele num: 109128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.855G>C
  hgvsp: ENSP00000455838.1:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.855G>C
  hgvsp: ENSP00000268058.3:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.855G>C
  hgvsp: ENSP00000456277.1:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.100G>C
  hgvsp: ENSP00000457669.1:p.Gln34His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.855G>C
  hgvsp: ENSP00000378564.2:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.855G>C
  hgvsp: ENSP00000378567.3:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.855G>C
  hgvsp: ENSP00000456486.1:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.176G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.855G>C
  hgvsp: ENSP00000315434.8:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.855G>C
  hgvsp: ENSP00000455612.1:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.855G>C
  hgvsp: ENSP00000457032.1:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.855G>C
  hgvsp: ENSP00000394642.3:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.855G>C
  hgvsp: ENSP00000457023.1:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.855G>C
  hgvsp: ENSP00000353004.4:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.169G>C
  hgvsp: ENSP00000456989.1:p.Gln57His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.855G>C
  hgvsp: ENSP00000395576.2:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.706G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.855G>C
  hgvsp: ENSP00000268059.6:p.Gln285His
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln285His
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-74315422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315422
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315422
    reference: chr 15
allele count: 1
allele frequency: 9.158180086453219e-6
allele num: 109192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.856G>A
  hgvsp: ENSP00000455838.1:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.856G>A
  hgvsp: ENSP00000455612.1:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.856G>A
  hgvsp: ENSP00000268058.3:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.856G>A
  hgvsp: ENSP00000395576.2:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.856G>A
  hgvsp: ENSP00000378564.2:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.101G>A
  hgvsp: ENSP00000457669.1:p.Val35Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.856G>A
  hgvsp: ENSP00000315434.8:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.856G>A
  hgvsp: ENSP00000456277.1:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.856G>A
  hgvsp: ENSP00000457032.1:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.170G>A
  hgvsp: ENSP00000456989.1:p.Val58Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.856G>A
  hgvsp: ENSP00000353004.4:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.856G>A
  hgvsp: ENSP00000378567.3:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.856G>A
  hgvsp: ENSP00000456486.1:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.856G>A
  hgvsp: ENSP00000457023.1:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.177G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.856G>A
  hgvsp: ENSP00000394642.3:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.707G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.856G>A
  hgvsp: ENSP00000268059.6:p.Val286Met
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val286Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

15-74315422-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315422
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315422
    reference: chr 15
allele count: 1
allele frequency: 9.158180086453219e-6
allele num: 109192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.856G>C
  hgvsp: ENSP00000378567.3:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.856G>C
  hgvsp: ENSP00000268058.3:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.856G>C
  hgvsp: ENSP00000455838.1:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.856G>C
  hgvsp: ENSP00000395576.2:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.856G>C
  hgvsp: ENSP00000378564.2:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.170G>C
  hgvsp: ENSP00000456989.1:p.Val58Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.856G>C
  hgvsp: ENSP00000456277.1:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.856G>C
  hgvsp: ENSP00000394642.3:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.177G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.856G>C
  hgvsp: ENSP00000457023.1:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.856G>C
  hgvsp: ENSP00000456486.1:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.856G>C
  hgvsp: ENSP00000457032.1:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.856G>C
  hgvsp: ENSP00000455612.1:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.856G>C
  hgvsp: ENSP00000353004.4:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.856G>C
  hgvsp: ENSP00000268059.6:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.101G>C
  hgvsp: ENSP00000457669.1:p.Val35Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.707G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.856G>C
  hgvsp: ENSP00000315434.8:p.Val286Leu
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14970
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val286Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

15-74315425-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315425
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315425
    reference: chr 15
allele count: 1
allele frequency: 9.147457006952068e-6
allele num: 109320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.859G>A
  hgvsp: ENSP00000315434.8:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.859G>A
  hgvsp: ENSP00000457023.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.859G>A
  hgvsp: ENSP00000456277.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.710G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.859G>A
  hgvsp: ENSP00000378567.3:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.859G>A
  hgvsp: ENSP00000395576.2:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.859G>A
  hgvsp: ENSP00000457032.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.859G>A
  hgvsp: ENSP00000455612.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.859G>A
  hgvsp: ENSP00000353004.4:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.859G>A
  hgvsp: ENSP00000394642.3:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.859G>A
  hgvsp: ENSP00000268058.3:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.180G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.859G>A
  hgvsp: ENSP00000378564.2:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.173G>A
  hgvsp: ENSP00000456989.1:p.Val59Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.859G>A
  hgvsp: ENSP00000455838.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.859G>A
  hgvsp: ENSP00000268059.6:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.104G>A
  hgvsp: ENSP00000457669.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.859G>A
  hgvsp: ENSP00000456486.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val287Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

15-74315435-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315435
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315435
    reference: chr 15
allele count: 1
allele frequency: 9.112281533050245e-6
allele num: 109742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.869T>G
  hgvsp: ENSP00000455838.1:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.869T>G
  hgvsp: ENSP00000456486.1:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.869T>G
  hgvsp: ENSP00000378567.3:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.869T>G
  hgvsp: ENSP00000457032.1:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.183T>G
  hgvsp: ENSP00000456989.1:p.Val62Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.869T>G
  hgvsp: ENSP00000395576.2:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.869T>G
  hgvsp: ENSP00000378564.2:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.869T>G
  hgvsp: ENSP00000268058.3:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.114T>G
  hgvsp: ENSP00000457669.1:p.Val39Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.869T>G
  hgvsp: ENSP00000455612.1:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.869T>G
  hgvsp: ENSP00000315434.8:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.869T>G
  hgvsp: ENSP00000457023.1:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.869T>G
  hgvsp: ENSP00000268059.6:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.869T>G
  hgvsp: ENSP00000394642.3:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.869T>G
  hgvsp: ENSP00000456277.1:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.190T>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.869T>G
  hgvsp: ENSP00000353004.4:p.Val290Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.720T>G
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val290Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

15-74315440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315440
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315440
    reference: chr 15
allele count: 1
allele frequency: 9.097028910357877e-6
allele num: 109926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.188G>A
  hgvsp: ENSP00000456989.1:p.Ala64Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.874G>A
  hgvsp: ENSP00000315434.8:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.874G>A
  hgvsp: ENSP00000457023.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.874G>A
  hgvsp: ENSP00000456486.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.874G>A
  hgvsp: ENSP00000378564.2:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.874G>A
  hgvsp: ENSP00000456277.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.874G>A
  hgvsp: ENSP00000268058.3:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.874G>A
  hgvsp: ENSP00000378567.3:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.874G>A
  hgvsp: ENSP00000268059.6:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.874G>A
  hgvsp: ENSP00000395576.2:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.874G>A
  hgvsp: ENSP00000394642.3:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.874G>A
  hgvsp: ENSP00000455612.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.874G>A
  hgvsp: ENSP00000353004.4:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.874G>A
  hgvsp: ENSP00000457032.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.874G>A
  hgvsp: ENSP00000455838.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.195G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.725G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.119G>A
  hgvsp: ENSP00000457669.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala292Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

15-74315444-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315444
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315444
    reference: chr 15
allele count: 1
allele frequency: 9.085457816219359e-6
allele num: 110066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.878A>T
  hgvsp: ENSP00000455612.1:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.878A>T
  hgvsp: ENSP00000457023.1:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.192A>T
  hgvsp: ENSP00000456989.1:p.Gln65Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.878A>T
  hgvsp: ENSP00000268059.6:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.878A>T
  hgvsp: ENSP00000456486.1:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.878A>T
  hgvsp: ENSP00000457032.1:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.878A>T
  hgvsp: ENSP00000455838.1:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.729A>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.878A>T
  hgvsp: ENSP00000394642.3:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.878A>T
  hgvsp: ENSP00000378564.2:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.878A>T
  hgvsp: ENSP00000353004.4:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.878A>T
  hgvsp: ENSP00000268058.3:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.878A>T
  hgvsp: ENSP00000378567.3:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.199A>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.878A>T
  hgvsp: ENSP00000456277.1:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.878A>T
  hgvsp: ENSP00000395576.2:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.123A>T
  hgvsp: ENSP00000457669.1:p.Gln42Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.878A>T
  hgvsp: ENSP00000315434.8:p.Gln293Leu
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln293Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

15-74315453-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315453
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315453
    reference: chr 15
allele count: 1
allele frequency: 9.053378720938654e-6
allele num: 110456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.887A>G
  hgvsp: ENSP00000378567.3:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.887A>G
  hgvsp: ENSP00000456486.1:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.201A>G
  hgvsp: ENSP00000456989.1:p.Glu68Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.132A>G
  hgvsp: ENSP00000457669.1:p.Glu45Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.887A>G
  hgvsp: ENSP00000395576.2:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.887A>G
  hgvsp: ENSP00000455612.1:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.887A>G
  hgvsp: ENSP00000315434.8:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.887A>G
  hgvsp: ENSP00000457032.1:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.887A>G
  hgvsp: ENSP00000394642.3:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.887A>G
  hgvsp: ENSP00000456277.1:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.887A>G
  hgvsp: ENSP00000268058.3:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.887A>G
  hgvsp: ENSP00000353004.4:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.887A>G
  hgvsp: ENSP00000455838.1:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.887A>G
  hgvsp: ENSP00000378564.2:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.208A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.887A>G
  hgvsp: ENSP00000268059.6:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.738A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.887A>G
  hgvsp: ENSP00000457023.1:p.Glu296Gly
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu296Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-74315455-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315455
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315455
    reference: chr 15
allele count: 1
allele frequency: 9.059448098421843e-6
allele num: 110382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.889C>T
  hgvsp: ENST00000565898.1:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.889C>T
  hgvsp: ENST00000436891.3:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.203C>T
  hgvsp: ENST00000565239.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.740C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.889C>T
  hgvsp: ENST00000268059.6:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.889C>T
  hgvsp: ENST00000359928.4:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.889C>T
  hgvsp: ENST00000435786.2:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.134C>T
  hgvsp: ENST00000567606.1:c.134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.889C>T
  hgvsp: ENST00000569477.1:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.889C>T
  hgvsp: ENST00000567543.1:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.889C>T
  hgvsp: ENST00000563500.1:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.889C>T
  hgvsp: ENST00000395132.2:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.889C>T
  hgvsp: ENST00000395135.3:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.210C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.889C>T
  hgvsp: ENST00000354026.6:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.889C>T
  hgvsp: ENST00000569965.1:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.889C>T
  hgvsp: ENST00000268058.3:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.889C>T
  hgvsp: ENST00000564428.1:c.889C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu297Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

15-74315457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315457
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315457
    reference: chr 15
allele count: 1
allele frequency: 9.05354265123943e-6
allele num: 110454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.212G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.891G>A
  hgvsp: ENST00000569477.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.891G>A
  hgvsp: ENST00000436891.3:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.891G>A
  hgvsp: ENST00000395135.3:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.891G>A
  hgvsp: ENST00000563500.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.891G>A
  hgvsp: ENST00000354026.6:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.891G>A
  hgvsp: ENST00000569965.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.891G>A
  hgvsp: ENST00000567543.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.891G>A
  hgvsp: ENST00000435786.2:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.891G>A
  hgvsp: ENST00000268058.3:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.891G>A
  hgvsp: ENST00000564428.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.891G>A
  hgvsp: ENST00000268059.6:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.891G>A
  hgvsp: ENST00000359928.4:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.891G>A
  hgvsp: ENST00000395132.2:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.136G>A
  hgvsp: ENST00000567606.1:c.136G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.742G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.891G>A
  hgvsp: ENST00000565898.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.205G>A
  hgvsp: ENST00000565239.1:c.205G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu297Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

15-74315474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315474
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315474
    reference: chr 15
allele count: 1
allele frequency: 9.030650026188885e-6
allele num: 110734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.908C>T
  hgvsp: ENSP00000455838.1:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.908C>T
  hgvsp: ENSP00000456486.1:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.908C>T
  hgvsp: ENSP00000455612.1:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.229C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.908C>T
  hgvsp: ENSP00000353004.4:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.908C>T
  hgvsp: ENSP00000395576.2:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.908C>T
  hgvsp: ENSP00000456277.1:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.908C>T
  hgvsp: ENSP00000394642.3:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.908C>T
  hgvsp: ENSP00000457032.1:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.153C>T
  hgvsp: ENSP00000457669.1:p.Ala52Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.759C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.908C>T
  hgvsp: ENSP00000457023.1:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.222C>T
  hgvsp: ENSP00000456989.1:p.Ala75Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.908C>T
  hgvsp: ENSP00000378564.2:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.908C>T
  hgvsp: ENSP00000378567.3:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.908C>T
  hgvsp: ENSP00000268059.6:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.908C>T
  hgvsp: ENSP00000268058.3:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.908C>T
  hgvsp: ENSP00000315434.8:p.Ala303Val
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala303Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

15-74315476-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315476
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315476
    reference: chr 15
allele count: 1
allele frequency: 9.02967150055081e-6
allele num: 110746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.910C>G
  hgvsp: ENSP00000394642.3:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.224C>G
  hgvsp: ENSP00000456989.1:p.Arg76Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.910C>G
  hgvsp: ENSP00000268059.6:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.155C>G
  hgvsp: ENSP00000457669.1:p.Arg53Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.910C>G
  hgvsp: ENSP00000457023.1:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.910C>G
  hgvsp: ENSP00000455612.1:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.761C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.910C>G
  hgvsp: ENSP00000268058.3:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.910C>G
  hgvsp: ENSP00000378567.3:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.910C>G
  hgvsp: ENSP00000455838.1:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.910C>G
  hgvsp: ENSP00000456486.1:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.910C>G
  hgvsp: ENSP00000353004.4:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.910C>G
  hgvsp: ENSP00000378564.2:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.231C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.910C>G
  hgvsp: ENSP00000315434.8:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.910C>G
  hgvsp: ENSP00000395576.2:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.910C>G
  hgvsp: ENSP00000456277.1:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.910C>G
  hgvsp: ENSP00000457032.1:p.Arg304Gly
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg304Gly
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-74315476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315476
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315476
    reference: chr 15
allele count: 1
allele frequency: 9.02967150055081e-6
allele num: 110746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.910C>T
  hgvsp: ENSP00000395576.2:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.910C>T
  hgvsp: ENSP00000268058.3:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.910C>T
  hgvsp: ENSP00000457023.1:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.910C>T
  hgvsp: ENSP00000315434.8:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.155C>T
  hgvsp: ENSP00000457669.1:p.Arg53Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.910C>T
  hgvsp: ENSP00000457032.1:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.910C>T
  hgvsp: ENSP00000378564.2:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.224C>T
  hgvsp: ENSP00000456989.1:p.Arg76Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.910C>T
  hgvsp: ENSP00000455612.1:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.761C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.910C>T
  hgvsp: ENSP00000268059.6:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.910C>T
  hgvsp: ENSP00000378567.3:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.231C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.910C>T
  hgvsp: ENSP00000455838.1:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.910C>T
  hgvsp: ENSP00000456486.1:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.910C>T
  hgvsp: ENSP00000456277.1:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.910C>T
  hgvsp: ENSP00000353004.4:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.910C>T
  hgvsp: ENSP00000394642.3:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg304Trp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

15-74315479-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315479
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315479
    reference: chr 15
allele count: 1
allele frequency: 9.019084382553484e-6
allele num: 110876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.227T>C
  hgvsp: ENSP00000456989.1:p.Tyr77His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.913T>C
  hgvsp: ENSP00000353004.4:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.913T>C
  hgvsp: ENSP00000394642.3:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.913T>C
  hgvsp: ENSP00000456277.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.913T>C
  hgvsp: ENSP00000378564.2:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.913T>C
  hgvsp: ENSP00000455838.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.158T>C
  hgvsp: ENSP00000457669.1:p.Tyr54His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.234T>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.913T>C
  hgvsp: ENSP00000455612.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.913T>C
  hgvsp: ENSP00000395576.2:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.913T>C
  hgvsp: ENSP00000457032.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.913T>C
  hgvsp: ENSP00000378567.3:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.913T>C
  hgvsp: ENSP00000456486.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.913T>C
  hgvsp: ENSP00000315434.8:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.764T>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.913T>C
  hgvsp: ENSP00000268059.6:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.913T>C
  hgvsp: ENSP00000457023.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.913T>C
  hgvsp: ENSP00000268058.3:p.Tyr305His
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr305His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-74315485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315485
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315485
    reference: chr 15
allele count: 104
allele frequency: 9.371564510606088e-4
allele num: 110974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.919C>T
  hgvsp: ENSP00000378567.3:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.919C>T
  hgvsp: ENSP00000353004.4:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.919C>T
  hgvsp: ENSP00000457032.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.919C>T
  hgvsp: ENSP00000456277.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.233C>T
  hgvsp: ENSP00000456989.1:p.Arg79Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.919C>T
  hgvsp: ENSP00000457023.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.919C>T
  hgvsp: ENSP00000455838.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.164C>T
  hgvsp: ENSP00000457669.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.919C>T
  hgvsp: ENSP00000378564.2:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.919C>T
  hgvsp: ENSP00000395576.2:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.919C>T
  hgvsp: ENSP00000268058.3:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.919C>T
  hgvsp: ENSP00000455612.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.919C>T
  hgvsp: ENSP00000315434.8:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.919C>T
  hgvsp: ENSP00000456486.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.919C>T
  hgvsp: ENSP00000394642.3:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.919C>T
  hgvsp: ENSP00000268059.6:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.770C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.240C>T
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg307Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

15-74315488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315488
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315488
    reference: chr 15
allele count: 2
allele frequency: 1.800633823105733e-5
allele num: 111072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.922G>A
  hgvsp: ENSP00000378567.3:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.922G>A
  hgvsp: ENSP00000268059.6:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.922G>A
  hgvsp: ENSP00000457023.1:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.922G>A
  hgvsp: ENSP00000457032.1:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.922G>A
  hgvsp: ENSP00000268058.3:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.922G>A
  hgvsp: ENSP00000456277.1:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.922G>A
  hgvsp: ENSP00000315434.8:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.922G>A
  hgvsp: ENSP00000395576.2:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.922G>A
  hgvsp: ENSP00000456486.1:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.922G>A
  hgvsp: ENSP00000394642.3:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.922G>A
  hgvsp: ENSP00000455612.1:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.167G>A
  hgvsp: ENSP00000457669.1:p.Asp57Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.922G>A
  hgvsp: ENSP00000378564.2:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.922G>A
  hgvsp: ENSP00000455838.1:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.773G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.922G>A
  hgvsp: ENSP00000353004.4:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.243G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.236G>A
  hgvsp: ENSP00000456989.1:p.Asp80Asn
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp308Asn
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

15-74315493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315493
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315493
    reference: chr 15
allele count: 5
allele frequency: 4.495270974934369e-5
allele num: 111228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.927C>T
  hgvsp: ENST00000563500.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.927C>T
  hgvsp: ENST00000569965.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.927C>T
  hgvsp: ENST00000268058.3:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.927C>T
  hgvsp: ENST00000435786.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.927C>T
  hgvsp: ENST00000395132.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.927C>T
  hgvsp: ENST00000268059.6:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.927C>T
  hgvsp: ENST00000569477.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.927C>T
  hgvsp: ENST00000395135.3:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.241C>T
  hgvsp: ENST00000565239.1:c.241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.172C>T
  hgvsp: ENST00000567606.1:c.172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.927C>T
  hgvsp: ENST00000359928.4:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.927C>T
  hgvsp: ENST00000436891.3:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.927C>T
  hgvsp: ENST00000564428.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.248C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.927C>T
  hgvsp: ENST00000354026.6:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.927C>T
  hgvsp: ENST00000565898.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.927C>T
  hgvsp: ENST00000567543.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.778C>T
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr309Tyr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

15-74315494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315494
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315494
    reference: chr 15
allele count: 6
allele frequency: 5.391416864351952e-5
allele num: 111288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.173G>A
  hgvsp: ENSP00000457669.1:p.Glu59Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.928G>A
  hgvsp: ENSP00000394642.3:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.249G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.928G>A
  hgvsp: ENSP00000457023.1:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.928G>A
  hgvsp: ENSP00000378567.3:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.928G>A
  hgvsp: ENSP00000457032.1:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.928G>A
  hgvsp: ENSP00000455612.1:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.928G>A
  hgvsp: ENSP00000395576.2:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.928G>A
  hgvsp: ENSP00000315434.8:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.928G>A
  hgvsp: ENSP00000456277.1:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.928G>A
  hgvsp: ENSP00000378564.2:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.928G>A
  hgvsp: ENSP00000456486.1:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.928G>A
  hgvsp: ENSP00000268058.3:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.928G>A
  hgvsp: ENSP00000455838.1:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.779G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.928G>A
  hgvsp: ENSP00000353004.4:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.242G>A
  hgvsp: ENSP00000456989.1:p.Glu82Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.928G>A
  hgvsp: ENSP00000268059.6:p.Glu310Lys
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu310Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-74315503-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315503
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315503
    reference: chr 15
allele count: 1
allele frequency: 8.987148377819717e-6
allele num: 111270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.937G>C
  hgvsp: ENSP00000353004.4:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.937G>C
  hgvsp: ENSP00000268058.3:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.937G>C
  hgvsp: ENSP00000268059.6:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.937G>C
  hgvsp: ENSP00000455838.1:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.937G>C
  hgvsp: ENSP00000457032.1:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.937G>C
  hgvsp: ENSP00000378567.3:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.251G>C
  hgvsp: ENSP00000456989.1:p.Ala85Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.937G>C
  hgvsp: ENSP00000378564.2:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.788G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.937G>C
  hgvsp: ENSP00000394642.3:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.182G>C
  hgvsp: ENSP00000457669.1:p.Ala62Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.937G>C
  hgvsp: ENSP00000456486.1:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.937G>C
  hgvsp: ENSP00000395576.2:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.937G>C
  hgvsp: ENSP00000456277.1:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.258G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.937G>C
  hgvsp: ENSP00000455612.1:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.937G>C
  hgvsp: ENSP00000315434.8:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.937G>C
  hgvsp: ENSP00000457023.1:p.Ala313Pro
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala313Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS

15-74315510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315510
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315510
    reference: chr 15
allele count: 1
allele frequency: 8.98069151324652e-6
allele num: 111350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.944G>A
  hgvsp: ENSP00000457023.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.795G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.944G>A
  hgvsp: ENSP00000268058.3:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.944G>A
  hgvsp: ENSP00000394642.3:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.944G>A
  hgvsp: ENSP00000378567.3:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.944G>A
  hgvsp: ENSP00000315434.8:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.944G>A
  hgvsp: ENSP00000457032.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.944G>A
  hgvsp: ENSP00000455612.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.944G>A
  hgvsp: ENSP00000395576.2:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.944G>A
  hgvsp: ENSP00000353004.4:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.258G>A
  hgvsp: ENSP00000456989.1:p.Arg87Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.944G>A
  hgvsp: ENSP00000378564.2:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.944G>A
  hgvsp: ENSP00000455838.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.944G>A
  hgvsp: ENSP00000456486.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.189G>A
  hgvsp: ENSP00000457669.1:p.Arg64Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.265G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.944G>A
  hgvsp: ENSP00000268059.6:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.944G>A
  hgvsp: ENSP00000456277.1:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg315Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

15-74315521-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315521
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315521
    reference: chr 15
allele count: 1
allele frequency: 8.960734063334468e-6
allele num: 111598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.955C>G
  hgvsp: ENSP00000268059.6:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.955C>G
  hgvsp: ENSP00000457032.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.955C>G
  hgvsp: ENSP00000378564.2:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.955C>G
  hgvsp: ENSP00000455838.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.955C>G
  hgvsp: ENSP00000315434.8:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.955C>G
  hgvsp: ENSP00000353004.4:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.955C>G
  hgvsp: ENSP00000395576.2:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.955C>G
  hgvsp: ENSP00000455612.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.200C>G
  hgvsp: ENSP00000457669.1:p.Leu68Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.955C>G
  hgvsp: ENSP00000378567.3:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.955C>G
  hgvsp: ENSP00000457023.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.269C>G
  hgvsp: ENSP00000456989.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.955C>G
  hgvsp: ENSP00000268058.3:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.806C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.276C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.955C>G
  hgvsp: ENSP00000456486.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.955C>G
  hgvsp: ENSP00000394642.3:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.955C>G
  hgvsp: ENSP00000456277.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu319Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

15-74315523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315523
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315523
    reference: chr 15
allele count: 6
allele frequency: 5.374321491911646e-5
allele num: 111642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.957G>A
  hgvsp: ENST00000354026.6:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.957G>A
  hgvsp: ENST00000359928.4:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.808G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.957G>A
  hgvsp: ENST00000436891.3:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.278G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.957G>A
  hgvsp: ENST00000564428.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.957G>A
  hgvsp: ENST00000565898.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.957G>A
  hgvsp: ENST00000268058.3:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.271G>A
  hgvsp: ENST00000565239.1:c.271G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.957G>A
  hgvsp: ENST00000435786.2:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.202G>A
  hgvsp: ENST00000567606.1:c.202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.957G>A
  hgvsp: ENST00000563500.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.957G>A
  hgvsp: ENST00000569477.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.957G>A
  hgvsp: ENST00000395135.3:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.957G>A
  hgvsp: ENST00000395132.2:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.957G>A
  hgvsp: ENST00000569965.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.957G>A
  hgvsp: ENST00000268059.6:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.957G>A
  hgvsp: ENST00000567543.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu319Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-74315524-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315524
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315524
    reference: chr 15
allele count: 1
allele frequency: 8.947585046795869e-6
allele num: 111762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.958G>T
  hgvsp: ENSP00000395576.2:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.958G>T
  hgvsp: ENSP00000353004.4:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.958G>T
  hgvsp: ENSP00000456486.1:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.958G>T
  hgvsp: ENSP00000268059.6:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.272G>T
  hgvsp: ENSP00000456989.1:p.Asp92Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.809G>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.958G>T
  hgvsp: ENSP00000455838.1:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.958G>T
  hgvsp: ENSP00000455612.1:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.958G>T
  hgvsp: ENSP00000378564.2:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.958G>T
  hgvsp: ENSP00000394642.3:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.203G>T
  hgvsp: ENSP00000457669.1:p.Asp69Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.958G>T
  hgvsp: ENSP00000457023.1:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.958G>T
  hgvsp: ENSP00000378567.3:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.958G>T
  hgvsp: ENSP00000456277.1:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.279G>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.958G>T
  hgvsp: ENSP00000315434.8:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.958G>T
  hgvsp: ENSP00000457032.1:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.958G>T
  hgvsp: ENSP00000268058.3:p.Asp320Tyr
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp320Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-74315525-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315525
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315525
    reference: chr 15
allele count: 1
allele frequency: 8.945824089315109e-6
allele num: 111784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.959A>T
  hgvsp: ENSP00000456277.1:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.959A>T
  hgvsp: ENSP00000268058.3:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.959A>T
  hgvsp: ENSP00000378567.3:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.959A>T
  hgvsp: ENSP00000378564.2:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.959A>T
  hgvsp: ENSP00000268059.6:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.959A>T
  hgvsp: ENSP00000315434.8:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.959A>T
  hgvsp: ENSP00000455838.1:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.959A>T
  hgvsp: ENSP00000353004.4:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.273A>T
  hgvsp: ENSP00000456989.1:p.Asp92Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.959A>T
  hgvsp: ENSP00000457032.1:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.959A>T
  hgvsp: ENSP00000395576.2:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.959A>T
  hgvsp: ENSP00000457023.1:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.959A>T
  hgvsp: ENSP00000394642.3:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.959A>T
  hgvsp: ENSP00000455612.1:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.959A>T
  hgvsp: ENSP00000456486.1:p.Asp320Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.204A>T
  hgvsp: ENSP00000457669.1:p.Asp69Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.280A>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.810A>T
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp320Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

15-74315532-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315532
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315532
    reference: chr 15
allele count: 1
allele frequency: 8.938148015731141e-6
allele num: 111880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.966G>A
  hgvsp: ENST00000569965.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.966G>A
  hgvsp: ENST00000395135.3:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.817G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.966G>A
  hgvsp: ENST00000268058.3:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.966G>A
  hgvsp: ENST00000268059.6:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.966G>A
  hgvsp: ENST00000563500.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.966G>A
  hgvsp: ENST00000359928.4:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.966G>A
  hgvsp: ENST00000435786.2:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.280G>A
  hgvsp: ENST00000565239.1:c.280G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.966G>A
  hgvsp: ENST00000395132.2:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.966G>A
  hgvsp: ENST00000569477.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.287G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.966G>A
  hgvsp: ENST00000354026.6:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.211G>A
  hgvsp: ENST00000567606.1:c.211G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.966G>A
  hgvsp: ENST00000564428.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.966G>A
  hgvsp: ENST00000565898.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.966G>A
  hgvsp: ENST00000436891.3:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.966G>A
  hgvsp: ENST00000567543.1:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29299
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val322Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

15-74315539-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315539
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315539
    reference: chr 15
allele count: 2
allele frequency: 1.786894912710184e-5
allele num: 111926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.973C>T
  hgvsp: ENSP00000394642.3:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.973C>T
  hgvsp: ENSP00000378567.3:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.973C>T
  hgvsp: ENSP00000353004.4:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.973C>T
  hgvsp: ENSP00000378564.2:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.973C>T
  hgvsp: ENSP00000457032.1:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.973C>T
  hgvsp: ENSP00000457023.1:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.973C>T
  hgvsp: ENSP00000456277.1:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.973C>T
  hgvsp: ENSP00000268058.3:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.218C>T
  hgvsp: ENSP00000457669.1:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.973C>T
  hgvsp: ENSP00000395576.2:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.973C>T
  hgvsp: ENSP00000455838.1:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.973C>T
  hgvsp: ENSP00000268059.6:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.973C>T
  hgvsp: ENSP00000455612.1:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.294C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.287C>T
  hgvsp: ENSP00000456989.1:p.Arg97Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.824C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.973C>T
  hgvsp: ENSP00000456486.1:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.973C>T
  hgvsp: ENSP00000315434.8:p.Arg325Cys
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg325Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

15-74315541-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315541
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315541
    reference: chr 15
allele count: 2
allele frequency: 1.783071518998627e-5
allele num: 112166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.975C>T
  hgvsp: ENST00000395132.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.975C>T
  hgvsp: ENST00000268058.3:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.975C>T
  hgvsp: ENST00000565898.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.220C>T
  hgvsp: ENST00000567606.1:c.220C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.975C>T
  hgvsp: ENST00000354026.6:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.289C>T
  hgvsp: ENST00000565239.1:c.289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.975C>T
  hgvsp: ENST00000563500.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.975C>T
  hgvsp: ENST00000359928.4:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.975C>T
  hgvsp: ENST00000435786.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.975C>T
  hgvsp: ENST00000569477.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.975C>T
  hgvsp: ENST00000564428.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.975C>T
  hgvsp: ENST00000395135.3:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.975C>T
  hgvsp: ENST00000436891.3:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.975C>T
  hgvsp: ENST00000268059.6:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.296C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.826C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.975C>T
  hgvsp: ENST00000569965.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.975C>T
  hgvsp: ENST00000567543.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg325Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

15-74315550-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315550
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315550
    reference: chr 15
allele count: 14
allele frequency: 1.245839785003649e-4
allele num: 112374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.984G>C
  hgvsp: ENST00000563500.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.984G>C
  hgvsp: ENST00000569477.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.984G>C
  hgvsp: ENST00000395135.3:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.984G>C
  hgvsp: ENST00000435786.2:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.984G>C
  hgvsp: ENST00000436891.3:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.984G>C
  hgvsp: ENST00000268059.6:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.229G>C
  hgvsp: ENST00000567606.1:c.229G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.984G>C
  hgvsp: ENST00000268058.3:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.305G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.984G>C
  hgvsp: ENST00000359928.4:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.984G>C
  hgvsp: ENST00000565898.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.984G>C
  hgvsp: ENST00000567543.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.835G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.984G>C
  hgvsp: ENST00000564428.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.984G>C
  hgvsp: ENST00000395132.2:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.298G>C
  hgvsp: ENST00000565239.1:c.298G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.984G>C
  hgvsp: ENST00000354026.6:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.984G>C
  hgvsp: ENST00000569965.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr328Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

15-74315557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315557
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315557
    reference: chr 15
allele count: 1
allele frequency: 8.868550346760318e-6
allele num: 112758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.312G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.991G>A
  hgvsp: ENSP00000315434.8:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.991G>A
  hgvsp: ENSP00000455838.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.991G>A
  hgvsp: ENSP00000394642.3:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.991G>A
  hgvsp: ENSP00000395576.2:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.991G>A
  hgvsp: ENSP00000378564.2:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.991G>A
  hgvsp: ENSP00000455612.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.991G>A
  hgvsp: ENSP00000456486.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.305G>A
  hgvsp: ENSP00000456989.1:p.Ala103Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.991G>A
  hgvsp: ENSP00000353004.4:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.991G>A
  hgvsp: ENSP00000268058.3:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.991G>A
  hgvsp: ENSP00000457032.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.991G>A
  hgvsp: ENSP00000378567.3:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.991G>A
  hgvsp: ENSP00000268059.6:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.991G>A
  hgvsp: ENSP00000456277.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.991G>A
  hgvsp: ENSP00000457023.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.236G>A
  hgvsp: ENSP00000457669.1:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.842G>A
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala331Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

15-74315558-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315558
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315558
    reference: chr 15
allele count: 2
allele frequency: 1.772735330615139e-5
allele num: 112820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.992C>T
  hgvsp: ENSP00000395576.2:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.992C>T
  hgvsp: ENSP00000456277.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.992C>T
  hgvsp: ENSP00000378564.2:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.992C>T
  hgvsp: ENSP00000456486.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.992C>T
  hgvsp: ENSP00000353004.4:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.992C>T
  hgvsp: ENSP00000455612.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.306C>T
  hgvsp: ENSP00000456989.1:p.Ala103Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.313C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.992C>T
  hgvsp: ENSP00000315434.8:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.992C>T
  hgvsp: ENSP00000455838.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.992C>T
  hgvsp: ENSP00000268059.6:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.992C>T
  hgvsp: ENSP00000378567.3:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.992C>T
  hgvsp: ENSP00000268058.3:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.992C>T
  hgvsp: ENSP00000457032.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.992C>T
  hgvsp: ENSP00000457023.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.992C>T
  hgvsp: ENSP00000394642.3:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.843C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.237C>T
  hgvsp: ENSP00000457669.1:p.Ala80Val
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala331Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

15-74315565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315565
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315565
    reference: chr 15
allele count: 46
allele frequency: 4.063029960429621e-4
allele num: 113216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.244G>A
  hgvsp: ENST00000567606.1:c.244G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.999G>A
  hgvsp: ENST00000563500.1:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.999G>A
  hgvsp: ENST00000268058.3:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.999G>A
  hgvsp: ENST00000435786.2:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.999G>A
  hgvsp: ENST00000359928.4:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.999G>A
  hgvsp: ENST00000567543.1:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.999G>A
  hgvsp: ENST00000395135.3:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.999G>A
  hgvsp: ENST00000569965.1:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.999G>A
  hgvsp: ENST00000436891.3:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.999G>A
  hgvsp: ENST00000395132.2:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.320G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.999G>A
  hgvsp: ENST00000268059.6:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.999G>A
  hgvsp: ENST00000569477.1:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.313G>A
  hgvsp: ENST00000565239.1:c.313G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.999G>A
  hgvsp: ENST00000564428.1:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.850G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.999G>A
  hgvsp: ENST00000354026.6:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.999G>A
  hgvsp: ENST00000565898.1:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val333Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

15-74315580-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315580
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315580
    reference: chr 15
allele count: 4
allele frequency: 3.519329919583311e-5
allele num: 113658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1014C>G
  hgvsp: ENSP00000394642.3:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1014C>G
  hgvsp: ENSP00000457023.1:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1014C>G
  hgvsp: ENSP00000456486.1:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1014C>G
  hgvsp: ENSP00000378567.3:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.865C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.335C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.328C>G
  hgvsp: ENSP00000456989.1:p.Cys110Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1014C>G
  hgvsp: ENSP00000455838.1:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1014C>G
  hgvsp: ENSP00000455612.1:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1014C>G
  hgvsp: ENSP00000353004.4:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1014C>G
  hgvsp: ENSP00000315434.8:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1014C>G
  hgvsp: ENSP00000378564.2:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1014C>G
  hgvsp: ENSP00000457032.1:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1014C>G
  hgvsp: ENSP00000268059.6:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1014C>G
  hgvsp: ENSP00000395576.2:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1014C>G
  hgvsp: ENSP00000268058.3:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1014C>G
  hgvsp: ENSP00000456277.1:p.Cys338Trp
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.259C>G
  hgvsp: ENSP00000457669.1:p.Cys87Trp
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys338Trp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS

15-74315592-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315592
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315592
    reference: chr 15
allele count: 1
allele frequency: 8.785339026233022e-6
allele num: 113826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1026C>T
  hgvsp: ENST00000436891.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.877C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1026C>T
  hgvsp: ENST00000565898.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1026C>T
  hgvsp: ENST00000395135.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1026C>T
  hgvsp: ENST00000564428.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.271C>T
  hgvsp: ENST00000567606.1:c.271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.340C>T
  hgvsp: ENST00000565239.1:c.340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1026C>T
  hgvsp: ENST00000569965.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1026C>T
  hgvsp: ENST00000354026.6:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1026C>T
  hgvsp: ENST00000435786.2:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1026C>T
  hgvsp: ENST00000563500.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1026C>T
  hgvsp: ENST00000569477.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1026C>T
  hgvsp: ENST00000268058.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1026C>T
  hgvsp: ENST00000567543.1:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1026C>T
  hgvsp: ENST00000395132.2:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1026C>T
  hgvsp: ENST00000268059.6:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.347C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1026C>T
  hgvsp: ENST00000359928.4:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp342Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-74315599-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315599
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315599
    reference: chr 15
allele count: 15
allele frequency: 1.316158921802611e-4
allele num: 113968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1033G>A
  hgvsp: ENSP00000353004.4:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.347G>A
  hgvsp: ENSP00000456989.1:p.Val117Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1033G>A
  hgvsp: ENSP00000315434.8:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1033G>A
  hgvsp: ENSP00000455612.1:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1033G>A
  hgvsp: ENSP00000457032.1:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1033G>A
  hgvsp: ENSP00000457023.1:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1033G>A
  hgvsp: ENSP00000455838.1:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1033G>A
  hgvsp: ENSP00000394642.3:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1033G>A
  hgvsp: ENSP00000395576.2:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.354G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1033G>A
  hgvsp: ENSP00000456277.1:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1033G>A
  hgvsp: ENSP00000378567.3:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1033G>A
  hgvsp: ENSP00000378564.2:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1033G>A
  hgvsp: ENSP00000268059.6:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.884G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.278G>A
  hgvsp: ENSP00000457669.1:p.Val94Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1033G>A
  hgvsp: ENSP00000456486.1:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1033G>A
  hgvsp: ENSP00000268058.3:p.Val345Met
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val345Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

15-74315604-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315604
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315604
    reference: chr 15
allele count: 2
allele frequency: 1.755032555853911e-5
allele num: 113958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1038G>T
  hgvsp: ENST00000563500.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1038G>T
  hgvsp: ENST00000268058.3:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1038G>T
  hgvsp: ENST00000395132.2:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.889G>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1038G>T
  hgvsp: ENST00000564428.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1038G>T
  hgvsp: ENST00000569477.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1038G>T
  hgvsp: ENST00000395135.3:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1038G>T
  hgvsp: ENST00000565898.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1038G>T
  hgvsp: ENST00000435786.2:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1038G>T
  hgvsp: ENST00000436891.3:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1038G>T
  hgvsp: ENST00000569965.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.352G>T
  hgvsp: ENST00000565239.1:c.352G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.283G>T
  hgvsp: ENST00000567606.1:c.283G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1038G>T
  hgvsp: ENST00000567543.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.359G>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1038G>T
  hgvsp: ENST00000268059.6:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1038G>T
  hgvsp: ENST00000359928.4:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1038G>T
  hgvsp: ENST00000354026.6:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu346Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

15-74315606-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315606
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315606
    reference: chr 15
allele count: 1
allele frequency: 8.770391159445711e-6
allele num: 114020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.354A>G
  hgvsp: ENSP00000456989.1:p.Asp119Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1040A>G
  hgvsp: ENSP00000315434.8:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.361A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.285A>G
  hgvsp: ENSP00000457669.1:p.Asp96Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1040A>G
  hgvsp: ENSP00000457032.1:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1040A>G
  hgvsp: ENSP00000457023.1:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1040A>G
  hgvsp: ENSP00000268058.3:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1040A>G
  hgvsp: ENSP00000378567.3:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1040A>G
  hgvsp: ENSP00000394642.3:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1040A>G
  hgvsp: ENSP00000456277.1:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.891A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1040A>G
  hgvsp: ENSP00000378564.2:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1040A>G
  hgvsp: ENSP00000268059.6:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1040A>G
  hgvsp: ENSP00000395576.2:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1040A>G
  hgvsp: ENSP00000456486.1:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1040A>G
  hgvsp: ENSP00000455612.1:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1040A>G
  hgvsp: ENSP00000455838.1:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1040A>G
  hgvsp: ENSP00000353004.4:p.Asp347Gly
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp347Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

15-74315608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315608
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315608
    reference: chr 15
allele count: 2
allele frequency: 1.75435518675111e-5
allele num: 114002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1042A>G
  hgvsp: ENSP00000455612.1:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1042A>G
  hgvsp: ENSP00000315434.8:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1042A>G
  hgvsp: ENSP00000394642.3:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1042A>G
  hgvsp: ENSP00000268058.3:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.356A>G
  hgvsp: ENSP00000456989.1:p.Met120Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1042A>G
  hgvsp: ENSP00000395576.2:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.287A>G
  hgvsp: ENSP00000457669.1:p.Met97Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1042A>G
  hgvsp: ENSP00000378564.2:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1042A>G
  hgvsp: ENSP00000378567.3:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1042A>G
  hgvsp: ENSP00000456277.1:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1042A>G
  hgvsp: ENSP00000457032.1:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1042A>G
  hgvsp: ENSP00000268059.6:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1042A>G
  hgvsp: ENSP00000455838.1:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1042A>G
  hgvsp: ENSP00000353004.4:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1042A>G
  hgvsp: ENSP00000456486.1:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.893A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.363A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1042A>G
  hgvsp: ENSP00000457023.1:p.Met348Val
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met348Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

15-74315613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315613
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315613
    reference: chr 15
allele count: 1
allele frequency: 8.792445530799936e-6
allele num: 113734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1047C>T
  hgvsp: ENST00000569965.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1047C>T
  hgvsp: ENST00000563500.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1047C>T
  hgvsp: ENST00000359928.4:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1047C>T
  hgvsp: ENST00000436891.3:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1047C>T
  hgvsp: ENST00000565898.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1047C>T
  hgvsp: ENST00000567543.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1047C>T
  hgvsp: ENST00000268058.3:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.898C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1047C>T
  hgvsp: ENST00000564428.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1047C>T
  hgvsp: ENST00000354026.6:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.361C>T
  hgvsp: ENST00000565239.1:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1047C>T
  hgvsp: ENST00000569477.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1047C>T
  hgvsp: ENST00000395135.3:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1047C>T
  hgvsp: ENST00000435786.2:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1047C>T
  hgvsp: ENST00000395132.2:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.368C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.292C>T
  hgvsp: ENST00000567606.1:c.292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1047C>T
  hgvsp: ENST00000268059.6:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His349His
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

15-74315614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315614
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315614
    reference: chr 15
allele count: 1
allele frequency: 8.78981787497363e-6
allele num: 113768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1048G>A
  hgvsp: ENSP00000394642.3:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.362G>A
  hgvsp: ENSP00000456989.1:p.Gly122Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1048G>A
  hgvsp: ENSP00000378567.3:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1048G>A
  hgvsp: ENSP00000268058.3:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1048G>A
  hgvsp: ENSP00000268059.6:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1048G>A
  hgvsp: ENSP00000457023.1:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1048G>A
  hgvsp: ENSP00000455838.1:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.369G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1048G>A
  hgvsp: ENSP00000395576.2:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1048G>A
  hgvsp: ENSP00000455612.1:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1048G>A
  hgvsp: ENSP00000378564.2:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1048G>A
  hgvsp: ENSP00000457032.1:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1048G>A
  hgvsp: ENSP00000456486.1:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.293G>A
  hgvsp: ENSP00000457669.1:p.Gly99Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1048G>A
  hgvsp: ENSP00000456277.1:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.899G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1048G>A
  hgvsp: ENSP00000315434.8:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1048G>A
  hgvsp: ENSP00000353004.4:p.Gly350Ser
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly350Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

15-74315618-TCCTGCGCCAGGCGCTCTGCCG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315618
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315597
    reference: chr 15
allele count: 1
allele frequency: 8.795848359574281e-6
allele num: 113690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsp: ENSP00000455612.1:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsp: ENSP00000456486.1:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsp: ENSP00000268059.6:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsp: ENSP00000457669.1:p.Ala104_Gln110del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsp: ENSP00000395576.2:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsp: ENSP00000353004.4:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsp: ENSP00000455838.1:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsp: ENSP00000315434.8:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsp: ENSP00000268058.3:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsp: ENSP00000457032.1:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsp: ENSP00000394642.3:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsp: ENSP00000378567.3:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsp: ENSP00000378564.2:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsp: ENSP00000456989.1:p.Ala127_Gln133del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsp: ENSP00000457023.1:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsp: ENSP00000456277.1:p.Ala355_Gln361del
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala355_Gln361del
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: TCCTGCGCCAGGCGCTCTGCCG
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

15-74315631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315631
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315631
    reference: chr 15
allele count: 1
allele frequency: 8.866034222892101e-6
allele num: 112790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.916G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.386G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1065G>A
  hgvsp: ENST00000268059.6:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1065G>A
  hgvsp: ENST00000569477.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1065G>A
  hgvsp: ENST00000268058.3:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1065G>A
  hgvsp: ENST00000569965.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1065G>A
  hgvsp: ENST00000354026.6:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1065G>A
  hgvsp: ENST00000567543.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1065G>A
  hgvsp: ENST00000395135.3:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1065G>A
  hgvsp: ENST00000565898.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.379G>A
  hgvsp: ENST00000565239.1:c.379G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1065G>A
  hgvsp: ENST00000435786.2:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1065G>A
  hgvsp: ENST00000564428.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1065G>A
  hgvsp: ENST00000563500.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1065G>A
  hgvsp: ENST00000395132.2:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1065G>A
  hgvsp: ENST00000359928.4:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1065G>A
  hgvsp: ENST00000436891.3:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.310G>A
  hgvsp: ENST00000567606.1:c.310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala355Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

15-74315634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315634
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315634
    reference: chr 15
allele count: 2
allele frequency: 1.778346848769384e-5
allele num: 112464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.382C>T
  hgvsp: ENST00000565239.1:c.382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1068C>T
  hgvsp: ENST00000268058.3:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1068C>T
  hgvsp: ENST00000435786.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1068C>T
  hgvsp: ENST00000395132.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1068C>T
  hgvsp: ENST00000569477.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1068C>T
  hgvsp: ENST00000565898.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1068C>T
  hgvsp: ENST00000359928.4:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.389C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.313C>T
  hgvsp: ENST00000567606.1:c.313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1068C>T
  hgvsp: ENST00000354026.6:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1068C>T
  hgvsp: ENST00000436891.3:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1068C>T
  hgvsp: ENST00000395135.3:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1068C>T
  hgvsp: ENST00000563500.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1068C>T
  hgvsp: ENST00000569965.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1068C>T
  hgvsp: ENST00000564428.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1068C>T
  hgvsp: ENST00000268059.6:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.919C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1068C>T
  hgvsp: ENST00000567543.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu356Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

15-74315640-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315640
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315640
    reference: chr 15
allele count: 1
allele frequency: 8.874689385871495e-6
allele num: 112680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1074C>G
  hgvsp: ENST00000567543.1:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1074C>G
  hgvsp: ENST00000435786.2:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1074C>G
  hgvsp: ENST00000436891.3:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.319C>G
  hgvsp: ENST00000567606.1:c.319C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1074C>G
  hgvsp: ENST00000395132.2:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1074C>G
  hgvsp: ENST00000563500.1:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1074C>G
  hgvsp: ENST00000268058.3:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1074C>G
  hgvsp: ENST00000564428.1:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.5C>G
  hgvsp: ENST00000566068.1:c.5C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.925C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.388C>G
  hgvsp: ENST00000565239.1:c.388C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1074C>G
  hgvsp: ENST00000354026.6:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1074C>G
  hgvsp: ENST00000565898.1:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1074C>G
  hgvsp: ENST00000395135.3:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1074C>G
  hgvsp: ENST00000569477.1:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.395C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1074C>G
  hgvsp: ENST00000359928.4:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1074C>G
  hgvsp: ENST00000268059.6:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1074C>G
  hgvsp: ENST00000569965.1:c.1074C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg358Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

15-74315645-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315645
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315645
    reference: chr 15
allele count: 5
allele frequency: 4.443496498524759e-5
allele num: 112524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1079G>A
  hgvsp: ENSP00000457032.1:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.400G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1079G>A
  hgvsp: ENSP00000457023.1:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1079G>A
  hgvsp: ENSP00000378567.3:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1079G>A
  hgvsp: ENSP00000315434.8:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1079G>A
  hgvsp: ENSP00000353004.4:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1079G>A
  hgvsp: ENSP00000395576.2:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1079G>A
  hgvsp: ENSP00000455838.1:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1079G>A
  hgvsp: ENSP00000378564.2:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1079G>A
  hgvsp: ENSP00000455612.1:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1079G>A
  hgvsp: ENSP00000268058.3:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1079G>A
  hgvsp: ENSP00000456486.1:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.930G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1079G>A
  hgvsp: ENSP00000456277.1:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.393G>A
  hgvsp: ENSP00000456989.1:p.Arg132His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1079G>A
  hgvsp: ENSP00000268059.6:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1079G>A
  hgvsp: ENSP00000394642.3:p.Arg360His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.324G>A
  hgvsp: ENSP00000457669.1:p.Arg109His
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.10G>A
  hgvsp: ENSP00000458061.1:p.Arg4His
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg360His
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

15-74315650-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315650
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315650
    reference: chr 15
allele count: 1
allele frequency: 8.870753126940477e-6
allele num: 112730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.329G>C
  hgvsp: ENSP00000457669.1:p.Glu111Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1084G>C
  hgvsp: ENSP00000378567.3:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1084G>C
  hgvsp: ENSP00000353004.4:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1084G>C
  hgvsp: ENSP00000457023.1:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.935G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1084G>C
  hgvsp: ENSP00000457032.1:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1084G>C
  hgvsp: ENSP00000315434.8:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1084G>C
  hgvsp: ENSP00000268058.3:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1084G>C
  hgvsp: ENSP00000394642.3:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1084G>C
  hgvsp: ENSP00000378564.2:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1084G>C
  hgvsp: ENSP00000455612.1:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.15G>C
  hgvsp: ENSP00000458061.1:p.Glu6Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1084G>C
  hgvsp: ENSP00000456277.1:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.398G>C
  hgvsp: ENSP00000456989.1:p.Glu134Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.405G>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1084G>C
  hgvsp: ENSP00000456486.1:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1084G>C
  hgvsp: ENSP00000268059.6:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1084G>C
  hgvsp: ENSP00000455838.1:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1084G>C
  hgvsp: ENSP00000395576.2:p.Glu362Gln
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu362Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

15-74315651-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315651
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315651
    reference: chr 15
allele count: 5
allele frequency: 4.438762828024573e-5
allele num: 112644
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1085A>T
  hgvsp: ENSP00000268058.3:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.399A>T
  hgvsp: ENSP00000456989.1:p.Glu134Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1085A>T
  hgvsp: ENSP00000378564.2:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1085A>T
  hgvsp: ENSP00000455838.1:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1085A>T
  hgvsp: ENSP00000378567.3:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1085A>T
  hgvsp: ENSP00000456277.1:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.16A>T
  hgvsp: ENSP00000458061.1:p.Glu6Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1085A>T
  hgvsp: ENSP00000394642.3:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1085A>T
  hgvsp: ENSP00000455612.1:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1085A>T
  hgvsp: ENSP00000457032.1:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1085A>T
  hgvsp: ENSP00000456486.1:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1085A>T
  hgvsp: ENSP00000268059.6:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.406A>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1085A>T
  hgvsp: ENSP00000315434.8:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1085A>T
  hgvsp: ENSP00000395576.2:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1085A>T
  hgvsp: ENSP00000353004.4:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1085A>T
  hgvsp: ENSP00000457023.1:p.Glu362Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.330A>T
  hgvsp: ENSP00000457669.1:p.Glu111Val
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.936A>T
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu362Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/15-74315657-C-CCCAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315657
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315661
    reference: chr 15
allele count: 1
allele frequency: 8.869966294128083e-6
allele num: 112740
alternate allele: CCCAA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1094_1095insACCA
  hgvsp: ENSP00000378564.2:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1094_1095insACCA
  hgvsp: ENSP00000378567.3:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.945_946insACCA
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.339_340insACCA
  hgvsp: ENSP00000457669.1:p.Ser115ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1094_1095insACCA
  hgvsp: ENSP00000455612.1:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1094_1095insACCA
  hgvsp: ENSP00000455838.1:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1094_1095insACCA
  hgvsp: ENSP00000268058.3:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.25_26insACCA
  hgvsp: ENSP00000458061.1:p.Ser10ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1094_1095insACCA
  hgvsp: ENSP00000456277.1:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1094_1095insACCA
  hgvsp: ENSP00000457023.1:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1094_1095insACCA
  hgvsp: ENSP00000394642.3:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1094_1095insACCA
  hgvsp: ENSP00000456486.1:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1094_1095insACCA
  hgvsp: ENSP00000353004.4:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.408_409insACCA
  hgvsp: ENSP00000456989.1:p.Ser138ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1094_1095insACCA
  hgvsp: ENSP00000395576.2:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1094_1095insACCA
  hgvsp: ENSP00000268059.6:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1094_1095insACCA
  hgvsp: ENSP00000315434.8:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1094_1095insACCA
  hgvsp: ENSP00000457032.1:p.Ser366ProfsTer51
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.415_416insACCA
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser366ProfsTer51
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-74315669-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315669
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315669
    reference: chr 15
allele count: 2
allele frequency: 1.778694793760339e-5
allele num: 112442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1103A>G
  hgvsp: ENSP00000315434.8:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1103A>G
  hgvsp: ENSP00000457032.1:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1103A>G
  hgvsp: ENSP00000394642.3:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1103A>G
  hgvsp: ENSP00000395576.2:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1103A>G
  hgvsp: ENSP00000378567.3:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1103A>G
  hgvsp: ENSP00000378564.2:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.417A>G
  hgvsp: ENSP00000456989.1:p.Gln140Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1103A>G
  hgvsp: ENSP00000455838.1:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.424A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.348A>G
  hgvsp: ENSP00000457669.1:p.Gln117Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1103A>G
  hgvsp: ENSP00000268058.3:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1103A>G
  hgvsp: ENSP00000268059.6:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1103A>G
  hgvsp: ENSP00000456486.1:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1103A>G
  hgvsp: ENSP00000455612.1:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1103A>G
  hgvsp: ENSP00000353004.4:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1103A>G
  hgvsp: ENSP00000456277.1:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.34A>G
  hgvsp: ENSP00000458061.1:p.Gln12Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1103A>G
  hgvsp: ENSP00000457023.1:p.Gln368Arg
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.954A>G
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln368Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

15-74315674-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315674
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315674
    reference: chr 15
allele count: 25
allele frequency: 2.226298822733182e-4
allele num: 112294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1108G>A
  hgvsp: ENSP00000457023.1:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1108G>A
  hgvsp: ENSP00000455838.1:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.422G>A
  hgvsp: ENSP00000456989.1:p.Ala142Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1108G>A
  hgvsp: ENSP00000455612.1:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.353G>A
  hgvsp: ENSP00000457669.1:p.Ala119Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1108G>A
  hgvsp: ENSP00000315434.8:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1108G>A
  hgvsp: ENSP00000456277.1:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1108G>A
  hgvsp: ENSP00000268058.3:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1108G>A
  hgvsp: ENSP00000268059.6:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.429G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1108G>A
  hgvsp: ENSP00000353004.4:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1108G>A
  hgvsp: ENSP00000378564.2:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1108G>A
  hgvsp: ENSP00000456486.1:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1108G>A
  hgvsp: ENSP00000378567.3:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.39G>A
  hgvsp: ENSP00000458061.1:p.Ala14Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1108G>A
  hgvsp: ENSP00000394642.3:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1108G>A
  hgvsp: ENSP00000457032.1:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.959G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1108G>A
  hgvsp: ENSP00000395576.2:p.Ala370Thr
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala370Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

15-74315676-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315676
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315676
    reference: chr 15
allele count: 2
allele frequency: 1.782817207751689e-5
allele num: 112182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1110C>G
  hgvsp: ENST00000359928.4:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1110C>G
  hgvsp: ENST00000563500.1:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1110C>G
  hgvsp: ENST00000567543.1:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.424C>G
  hgvsp: ENST00000565239.1:c.424C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.431C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1110C>G
  hgvsp: ENST00000565898.1:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1110C>G
  hgvsp: ENST00000564428.1:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.41C>G
  hgvsp: ENST00000566068.1:c.41C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1110C>G
  hgvsp: ENST00000569477.1:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1110C>G
  hgvsp: ENST00000395132.2:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1110C>G
  hgvsp: ENST00000436891.3:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1110C>G
  hgvsp: ENST00000268058.3:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.961C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1110C>G
  hgvsp: ENST00000395135.3:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.355C>G
  hgvsp: ENST00000567606.1:c.355C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1110C>G
  hgvsp: ENST00000268059.6:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1110C>G
  hgvsp: ENST00000354026.6:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1110C>G
  hgvsp: ENST00000569965.1:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1110C>G
  hgvsp: ENST00000435786.2:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala370Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

15-74315676-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315676
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315676
    reference: chr 15
allele count: 2
allele frequency: 1.782817207751689e-5
allele num: 112182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1110C>T
  hgvsp: ENST00000268059.6:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1110C>T
  hgvsp: ENST00000569965.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1110C>T
  hgvsp: ENST00000563500.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1110C>T
  hgvsp: ENST00000395135.3:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1110C>T
  hgvsp: ENST00000436891.3:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1110C>T
  hgvsp: ENST00000395132.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1110C>T
  hgvsp: ENST00000569477.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.41C>T
  hgvsp: ENST00000566068.1:c.41C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1110C>T
  hgvsp: ENST00000567543.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1110C>T
  hgvsp: ENST00000359928.4:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1110C>T
  hgvsp: ENST00000564428.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1110C>T
  hgvsp: ENST00000565898.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1110C>T
  hgvsp: ENST00000435786.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.424C>T
  hgvsp: ENST00000565239.1:c.424C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1110C>T
  hgvsp: ENST00000354026.6:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.431C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.355C>T
  hgvsp: ENST00000567606.1:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.961C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1110C>T
  hgvsp: ENST00000268058.3:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala370Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

15-74315677-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315677
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315677
    reference: chr 15
allele count: 2
allele frequency: 1.783039726125098e-5
allele num: 112168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1111G>T
  hgvsp: ENSP00000457023.1:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1111G>T
  hgvsp: ENSP00000378564.2:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1111G>T
  hgvsp: ENSP00000456277.1:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1111G>T
  hgvsp: ENSP00000456486.1:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1111G>T
  hgvsp: ENSP00000353004.4:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1111G>T
  hgvsp: ENSP00000394642.3:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1111G>T
  hgvsp: ENSP00000457032.1:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1111G>T
  hgvsp: ENSP00000395576.2:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.425G>T
  hgvsp: ENSP00000456989.1:p.Val143Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1111G>T
  hgvsp: ENSP00000378567.3:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1111G>T
  hgvsp: ENSP00000268058.3:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.432G>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1111G>T
  hgvsp: ENSP00000455838.1:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1111G>T
  hgvsp: ENSP00000455612.1:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.962G>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.356G>T
  hgvsp: ENSP00000457669.1:p.Val120Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1111G>T
  hgvsp: ENSP00000268059.6:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.42G>T
  hgvsp: ENSP00000458061.1:p.Val15Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1111G>T
  hgvsp: ENSP00000315434.8:p.Val371Leu
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val371Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

15-74315680-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315680
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315680
    reference: chr 15
allele count: 1
allele frequency: 8.925224469395405e-6
allele num: 112042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1114C>G
  hgvsp: ENSP00000315434.8:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1114C>G
  hgvsp: ENSP00000268058.3:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.359C>G
  hgvsp: ENSP00000457669.1:p.Arg121Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1114C>G
  hgvsp: ENSP00000378567.3:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1114C>G
  hgvsp: ENSP00000457032.1:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1114C>G
  hgvsp: ENSP00000395576.2:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.428C>G
  hgvsp: ENSP00000456989.1:p.Arg144Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.45C>G
  hgvsp: ENSP00000458061.1:p.Arg16Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1114C>G
  hgvsp: ENSP00000378564.2:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.965C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1114C>G
  hgvsp: ENSP00000394642.3:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1114C>G
  hgvsp: ENSP00000457023.1:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1114C>G
  hgvsp: ENSP00000353004.4:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1114C>G
  hgvsp: ENSP00000455612.1:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1114C>G
  hgvsp: ENSP00000456277.1:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1114C>G
  hgvsp: ENSP00000455838.1:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.435C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1114C>G
  hgvsp: ENSP00000456486.1:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1114C>G
  hgvsp: ENSP00000268059.6:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg372Gly
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

15-74315683-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315683
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315683
    reference: chr 15
allele count: 1
allele frequency: 8.92936869363336e-6
allele num: 111990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.431A>G
  hgvsp: ENSP00000456989.1:p.Thr145Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1117A>G
  hgvsp: ENSP00000378564.2:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.968A>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1117A>G
  hgvsp: ENSP00000457023.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1117A>G
  hgvsp: ENSP00000395576.2:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1117A>G
  hgvsp: ENSP00000455838.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.362A>G
  hgvsp: ENSP00000457669.1:p.Thr122Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1117A>G
  hgvsp: ENSP00000456486.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1117A>G
  hgvsp: ENSP00000456277.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1117A>G
  hgvsp: ENSP00000455612.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1117A>G
  hgvsp: ENSP00000268059.6:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1117A>G
  hgvsp: ENSP00000457032.1:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.48A>G
  hgvsp: ENSP00000458061.1:p.Thr17Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1117A>G
  hgvsp: ENSP00000378567.3:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1117A>G
  hgvsp: ENSP00000394642.3:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1117A>G
  hgvsp: ENSP00000353004.4:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1117A>G
  hgvsp: ENSP00000315434.8:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1117A>G
  hgvsp: ENSP00000268058.3:p.Thr373Ala
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.438A>G
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr373Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

15-74315691-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315691
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315691
    reference: chr 15
allele count: 1
allele frequency: 8.96571510543681e-6
allele num: 111536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1125C>G
  hgvsp: ENST00000567543.1:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1125C>G
  hgvsp: ENST00000569965.1:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1125C>G
  hgvsp: ENST00000395132.2:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1125C>G
  hgvsp: ENST00000359928.4:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1125C>G
  hgvsp: ENST00000395135.3:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1125C>G
  hgvsp: ENST00000563500.1:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1125C>G
  hgvsp: ENST00000435786.2:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1125C>G
  hgvsp: ENST00000569477.1:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1125C>G
  hgvsp: ENST00000354026.6:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.56C>G
  hgvsp: ENST00000566068.1:c.56C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1125C>G
  hgvsp: ENST00000565898.1:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1125C>G
  hgvsp: ENST00000268058.3:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1125C>G
  hgvsp: ENST00000436891.3:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.446C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.439C>G
  hgvsp: ENST00000565239.1:c.439C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1125C>G
  hgvsp: ENST00000268059.6:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.976C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.370C>G
  hgvsp: ENST00000567606.1:c.370C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1125C>G
  hgvsp: ENST00000564428.1:c.1125C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly375Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

15-74315691-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315691
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315691
    reference: chr 15
allele count: 1
allele frequency: 8.96571510543681e-6
allele num: 111536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1125C>T
  hgvsp: ENST00000395135.3:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1125C>T
  hgvsp: ENST00000359928.4:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1125C>T
  hgvsp: ENST00000436891.3:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1125C>T
  hgvsp: ENST00000564428.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.56C>T
  hgvsp: ENST00000566068.1:c.56C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1125C>T
  hgvsp: ENST00000435786.2:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.446C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1125C>T
  hgvsp: ENST00000565898.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1125C>T
  hgvsp: ENST00000569477.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.370C>T
  hgvsp: ENST00000567606.1:c.370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1125C>T
  hgvsp: ENST00000354026.6:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.976C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1125C>T
  hgvsp: ENST00000567543.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1125C>T
  hgvsp: ENST00000395132.2:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1125C>T
  hgvsp: ENST00000563500.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.439C>T
  hgvsp: ENST00000565239.1:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1125C>T
  hgvsp: ENST00000268059.6:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1125C>T
  hgvsp: ENST00000268058.3:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1125C>T
  hgvsp: ENST00000569965.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly375Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

15-74315692-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315692
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315692
    reference: chr 15
allele count: 1
allele frequency: 8.980368913554968e-6
allele num: 111354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1126T>C
  hgvsp: ENSP00000457032.1:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1126T>C
  hgvsp: ENSP00000268059.6:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1126T>C
  hgvsp: ENSP00000457023.1:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1126T>C
  hgvsp: ENSP00000455612.1:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.447T>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1126T>C
  hgvsp: ENSP00000455838.1:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.371T>C
  hgvsp: ENSP00000457669.1:p.Phe125Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1126T>C
  hgvsp: ENSP00000378564.2:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1126T>C
  hgvsp: ENSP00000395576.2:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1126T>C
  hgvsp: ENSP00000394642.3:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.57T>C
  hgvsp: ENSP00000458061.1:p.Phe20Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.440T>C
  hgvsp: ENSP00000456989.1:p.Phe148Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1126T>C
  hgvsp: ENSP00000315434.8:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.977T>C
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1126T>C
  hgvsp: ENSP00000353004.4:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1126T>C
  hgvsp: ENSP00000456486.1:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1126T>C
  hgvsp: ENSP00000378567.3:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1126T>C
  hgvsp: ENSP00000268058.3:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1126T>C
  hgvsp: ENSP00000456277.1:p.Phe376Leu
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe376Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

15-74315697-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315697
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315697
    reference: chr 15
allele count: 5
allele frequency: 4.500936194728503e-5
allele num: 111088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.376C>G
  hgvsp: ENSP00000457669.1:p.Asp126Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1131C>G
  hgvsp: ENSP00000457032.1:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1131C>G
  hgvsp: ENSP00000455612.1:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.445C>G
  hgvsp: ENSP00000456989.1:p.Asp149Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1131C>G
  hgvsp: ENSP00000378564.2:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1131C>G
  hgvsp: ENSP00000394642.3:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1131C>G
  hgvsp: ENSP00000457023.1:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1131C>G
  hgvsp: ENSP00000378567.3:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1131C>G
  hgvsp: ENSP00000353004.4:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.982C>G
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1131C>G
  hgvsp: ENSP00000268058.3:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1131C>G
  hgvsp: ENSP00000455838.1:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1131C>G
  hgvsp: ENSP00000456277.1:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.62C>G
  hgvsp: ENSP00000458061.1:p.Asp21Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1131C>G
  hgvsp: ENSP00000395576.2:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1131C>G
  hgvsp: ENSP00000315434.8:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1131C>G
  hgvsp: ENSP00000456486.1:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1131C>G
  hgvsp: ENSP00000268059.6:p.Asp377Glu
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.452C>G
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp377Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

15-74315697-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315697
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315697
    reference: chr 15
allele count: 8
allele frequency: 7.201497911565606e-5
allele num: 111088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.452C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1131C>T
  hgvsp: ENST00000395132.2:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1131C>T
  hgvsp: ENST00000565898.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1131C>T
  hgvsp: ENST00000268058.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1131C>T
  hgvsp: ENST00000395135.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1131C>T
  hgvsp: ENST00000436891.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1131C>T
  hgvsp: ENST00000354026.6:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1131C>T
  hgvsp: ENST00000359928.4:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.62C>T
  hgvsp: ENST00000566068.1:c.62C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1131C>T
  hgvsp: ENST00000569477.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1131C>T
  hgvsp: ENST00000435786.2:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.982C>T
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1131C>T
  hgvsp: ENST00000564428.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.376C>T
  hgvsp: ENST00000567606.1:c.376C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.445C>T
  hgvsp: ENST00000565239.1:c.445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1131C>T
  hgvsp: ENST00000268059.6:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1131C>T
  hgvsp: ENST00000569965.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1131C>T
  hgvsp: ENST00000563500.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1131C>T
  hgvsp: ENST00000567543.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp377Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

15-74315698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74315698
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74315698
    reference: chr 15
allele count: 4
allele frequency: 3.603019330198707e-5
allele num: 111018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455838
  ensembl transcript: ENST00000565898
  gene symbol: PML
  hgvsc: ENST00000565898.1:c.1132G>A
  hgvsp: ENSP00000455838.1:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000315434
  ensembl transcript: ENST00000354026
  gene symbol: PML
  hgvsc: ENST00000354026.6:c.1132G>A
  hgvsp: ENSP00000315434.8:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000395576
  ensembl transcript: ENST00000435786
  gene symbol: PML
  hgvsc: ENST00000435786.2:c.1132G>A
  hgvsp: ENSP00000395576.2:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457032
  ensembl transcript: ENST00000563500
  gene symbol: PML
  hgvsc: ENST00000563500.1:c.1132G>A
  hgvsp: ENSP00000457032.1:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456277
  ensembl transcript: ENST00000567543
  gene symbol: PML
  hgvsc: ENST00000567543.1:c.1132G>A
  hgvsp: ENSP00000456277.1:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378567
  ensembl transcript: ENST00000395135
  gene symbol: PML
  hgvsc: ENST00000395135.3:c.1132G>A
  hgvsp: ENSP00000378567.3:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456989
  ensembl transcript: ENST00000565239
  gene symbol: PML
  hgvsc: ENST00000565239.1:c.446G>A
  hgvsp: ENSP00000456989.1:p.Glu150Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268058
  ensembl transcript: ENST00000268058
  gene symbol: PML
  hgvsc: ENST00000268058.3:c.1132G>A
  hgvsp: ENSP00000268058.3:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000378564
  ensembl transcript: ENST00000395132
  gene symbol: PML
  hgvsc: ENST00000395132.2:c.1132G>A
  hgvsp: ENSP00000378564.2:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000458061
  ensembl transcript: ENST00000566068
  gene symbol: PML
  hgvsc: ENST00000566068.1:c.63G>A
  hgvsp: ENSP00000458061.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000456486
  ensembl transcript: ENST00000569965
  gene symbol: PML
  hgvsc: ENST00000569965.1:c.1132G>A
  hgvsp: ENSP00000456486.1:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000455612
  ensembl transcript: ENST00000569477
  gene symbol: PML
  hgvsc: ENST00000569477.1:c.1132G>A
  hgvsp: ENSP00000455612.1:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000394642
  ensembl transcript: ENST00000436891
  gene symbol: PML
  hgvsc: ENST00000436891.3:c.1132G>A
  hgvsp: ENSP00000394642.3:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000569161
  gene symbol: PML
  hgvsc: ENST00000569161.1:n.453G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457023
  ensembl transcript: ENST00000564428
  gene symbol: PML
  hgvsc: ENST00000564428.1:c.1132G>A
  hgvsp: ENSP00000457023.1:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000353004
  ensembl transcript: ENST00000359928
  gene symbol: PML
  hgvsc: ENST00000359928.4:c.1132G>A
  hgvsp: ENSP00000353004.4:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140464
  ensembl transcript: ENST00000564725
  gene symbol: PML
  hgvsc: ENST00000564725.1:n.983G>A
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000268059
  ensembl transcript: ENST00000268059
  gene symbol: PML
  hgvsc: ENST00000268059.6:c.1132G>A
  hgvsp: ENSP00000268059.6:p.Glu378Lys
  variant of: http://identifiers.org/hgnc/9113
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140464
  ensembl protein: ENSP00000457669
  ensembl transcript: ENST00000567606
  gene symbol: PML
  hgvsc: ENST00000567606.1:c.377G>A
  hgvsp: ENSP00000457669.1:p.Glu127Lys
  variant of: http://identifiers.org/hgnc/9113
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Glu378Lys
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 749
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1029
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 280
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1800
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2591
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31058
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3777
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3849
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 242
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 855
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.715148188803513e-5
allele num: 58304
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.778e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.369193e6

MQ
type: SiteQuality
SIO_000300: 5.871e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.807e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 9.15e0

GenotypeDepth
all individuals: 1031
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31761
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14809
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 469
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 748
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3317
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 607
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2673
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1352
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1954
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3515
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.689760054072322e-5
allele num: 59180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.389742e6

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 7.288e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.318e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.000000000000001e-2

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 416
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31970
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1974
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3182
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2665
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 373
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 280
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1030
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14945
bin: 2.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 743
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43664
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11076
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.274859765425803e-4
allele num: 7844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8108
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.75e0

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

DP
type: SiteQuality
SIO_000300: 1.394311e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.029e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

GenotypeDepth
all individuals: 3164
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1271
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 744
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 280
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14970
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31970
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 374
bin: 5.25e1
variant carriers: 1

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

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

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2674
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

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

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

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
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allele num: 59568
num of homozygotes: 0

Latino
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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: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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South Asian
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African
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Latino
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European (Non-Finnish)
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East Asian
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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QD
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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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Latino
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European (Non-Finnish)
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Other
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African
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FS
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QD
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VQSLOD
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MQ
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BaseQRankSum
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DP
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GenotypeQuality
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South Asian
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InbreedingCoeff
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FS
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MQ
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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ClippingRankSum
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DP
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QD
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FS
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MQ
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East Asian
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South Asian
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FS
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East Asian
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MQRankSum
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SIO_000300: 3.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.97021887334051e-5
allele num: 11148
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16206
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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.03e-1

ReadPosRankSum
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SIO_000300: 8.66e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

InbreedingCoeff
type: SiteQuality
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DP
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BaseQRankSum
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SIO_000300: 2.98e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 1.578e0

QD
type: SiteQuality
SIO_000300: 1.053e1

GenotypeDepth
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bin: 2.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 128
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.233045622688039e-4
allele num: 8110
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.57e-2

QD
type: SiteQuality
SIO_000300: 1.811e1

ClippingRankSum
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SIO_000300: 7.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 1.410561e6

FS
type: SiteQuality
SIO_000300: 2.215e0

InbreedingCoeff
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SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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variant carriers: 14

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
all individuals: 8
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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variant carriers: 6

GenotypeDepth
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variant carriers: 8

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 11

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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variant carriers: 5

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

GenotypeQuality
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GenotypeQuality
all individuals: 2056
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variant carriers: 105

GenotypeQuality
all individuals: 586
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 89
allele frequency: 1.467484500725498e-3
allele num: 60648
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.485914229319935e-4
allele num: 11146
num of homozygotes: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.538071065989848e-3
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 8.561643835616438e-4
allele num: 5840
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.678273663560569e-4
allele num: 8156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
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SIO_000300: 1.414372e6

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

BaseQRankSum
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SIO_000300: 1.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.308e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 18
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GenotypeDepth
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GenotypeDepth
all individuals: 749
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GenotypeDepth
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GenotypeDepth
all individuals: 5
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GenotypeDepth
all individuals: 1916
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.295435821387378e-5
allele num: 60690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.837e0

MQRankSum
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SIO_000300: 1.11e0

DP
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SIO_000300: 1.411444e6

InbreedingCoeff
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SIO_000300: -3.5e-3

FS
type: SiteQuality
SIO_000300: 7.61e-1

ReadPosRankSum
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SIO_000300: 2.39e0

VQSLOD
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SIO_000300: -1.242e-1

ClippingRankSum
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SIO_000300: -2.07e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 5

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

GenotypeQuality
all individuals: 852
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variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.848656642839536e-4
allele num: 16228
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.954154727793696e-5
allele num: 11168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.645548790521639e-5
allele num: 60770
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

QD
type: SiteQuality
SIO_000300: 1.302e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 4.198e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

DP
type: SiteQuality
SIO_000300: 1.411946e6

GenotypeDepth
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bin: 4.25e1
variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 280
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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East Asian
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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African
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QD
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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VQSLOD
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MQ
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DP
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European (Finnish)
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Latino
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African
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East Asian
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.635590448151783e-5
allele num: 61140
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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Latino
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East Asian
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South Asian
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Other
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.875e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 61212
num of homozygotes: 0

South Asian
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East Asian
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Other
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ClippingRankSum
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SIO_000300: -8.799999999999999e-2

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.954154727793696e-5
allele num: 11168
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 800
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

African
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allele count: 13
allele frequency: 1.515858208955224e-3
allele num: 8576
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5846
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61498
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.6e-3

VQSLOD
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QD
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ClippingRankSum
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MQ
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.753e0

BaseQRankSum
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SIO_000300: 2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.03e-1

DP
type: SiteQuality
SIO_000300: 1.418146e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8690
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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.621060822202049e-5
allele num: 61688
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

VQSLOD
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SIO_000300: -8.844e-1

BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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DP
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SIO_000300: 1.422235e6

FS
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SIO_000300: 4.041e0

QD
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SIO_000300: 1.553e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

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

East Asian
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allele count: 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: 802
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8710
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.240020736132711e-5
allele num: 61728
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ReadPosRankSum
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SIO_000300: -5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQ
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FS
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VQSLOD
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SIO_000300: 2.94e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

DP
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SIO_000300: 1.423201e6

MQRankSum
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SIO_000300: 6.6e-1

QD
type: SiteQuality
SIO_000300: 1.097e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 46

Latino
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allele frequency: 8.939746111210442e-5
allele num: 11186
num of homozygotes: 0

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

Other
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allele count: 0
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African
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allele count: 1
allele frequency: 1.125112511251125e-4
allele num: 8888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 28
allele frequency: 4.522694233564852e-4
allele num: 61910
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 16
allele frequency: 9.828009828009828e-4
allele num: 16280
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.827342065458758e-5
allele num: 62146
num of homozygotes: 0

European (Finnish)
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allele num: 5892
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Other
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South Asian
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East Asian
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.607096940087426e-5
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num of homozygotes: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62276
num of homozygotes: 0

East Asian
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Other
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num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.226993865030675e-4
allele num: 16300
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FS
type: SiteQuality
SIO_000300: 9.727e0

InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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SIO_000300: 5.963e1

ReadPosRankSum
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SIO_000300: 9.409999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Latino
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South Asian
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African
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Other
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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Latino
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QD
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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East Asian
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South Asian
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European (Finnish)
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African
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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QD
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DP
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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ReadPosRankSum
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MQ
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FS
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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European (Finnish)
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East Asian
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VQSLOD
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DP
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MQ
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQ
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DP
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SIO_000300: 1.445575e6

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 600
bin: 4.75e1
variant carriers: 1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 865
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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: 8.75e1
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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44536
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.159801553626216e-5
allele num: 61276
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

FS
type: SiteQuality
SIO_000300: 3.223e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 4.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 1.44605e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 6.75e1
variant carriers: 1

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 1942
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3939
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62903593653276e-5
allele num: 61386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.86e1

DP
type: SiteQuality
SIO_000300: 1.449818e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.063e0

QD
type: SiteQuality
SIO_000300: 1.031e1

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1223
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 598
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2960
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variant carriers: 0

GenotypeDepth
all individuals: 2915
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1644
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1000
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variant carriers: 1

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 1

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 278
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variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
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variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45057
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 191
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variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1945
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variant carriers: 5

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1290
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variant carriers: 0

GenotypeQuality
all individuals: 311
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variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 354
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variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.151287903488751e-5
allele num: 61340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8774
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.449394e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.17e1

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 138
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variant carriers: 0

GenotypeDepth
all individuals: 1007
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 3617
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 45321
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
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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: 75
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1939
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variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628187176397799e-5
allele num: 61418
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

FS
type: SiteQuality
SIO_000300: 7.521e0

MQ
type: SiteQuality
SIO_000300: 5.158e1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

BaseQRankSum
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SIO_000300: 3.07e-1

MQRankSum
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SIO_000300: -3.464e0

DP
type: SiteQuality
SIO_000300: 1.451533e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
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SIO_000300: -1.623e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 113
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 498
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.25e1
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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variant carriers: 0

GenotypeQuality
all individuals: 854
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 344
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variant carriers: 0

GenotypeQuality
all individuals: 1937
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variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.262642740619902e-5
allele num: 61300
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.447879e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

FS
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SIO_000300: 2.584e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Other
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Latino
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European (Non-Finnish)
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-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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QD
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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Other
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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Latino
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African
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East Asian
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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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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DP
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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South Asian
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DP
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MQ
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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Other
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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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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MQRankSum
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QD
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ReadPosRankSum
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MQ
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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Latino
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African
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European (Finnish)
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
all individuals: 75
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1316
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 28669
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18230
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2959
bin: 3.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1025
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 740
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 248
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 4448
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 44022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3711
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.794319294809011e-4
allele num: 8168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16020
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11060
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 1.869e0

DP
type: SiteQuality
SIO_000300: 1.434221e6

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 5.918e1

GenotypeDepth
all individuals: 276
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 554
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2963
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 28635
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 18203
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3656
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1336
bin: 2.5e0
variant carriers: 0