22-18907279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907279
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907279
    reference: chr 22
allele count: 2
allele frequency: 1.709372489359156e-5
allele num: 117002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1789C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1381C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.231C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1953C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3524C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1044C>T
  hgvsp: ENST00000357068.6:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.720C>T
  hgvsp: ENST00000334029.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1809C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.720C>T
  hgvsp: ENST00000420436.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe348Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

22-18907281-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907281
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907281
    reference: chr 22
allele count: 1
allele frequency: 8.557101538566857e-6
allele num: 116862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.718T>C
  hgvsp: ENSP00000410805.1:p.Phe240Leu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3522T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.718T>C
  hgvsp: ENSP00000334726.2:p.Phe240Leu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1042T>C
  hgvsp: ENSP00000349577.6:p.Phe348Leu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1787T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1951T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.229T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1379T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1807T>C
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32179
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe348Leu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

22-18907282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907282
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907282
    reference: chr 22
allele count: 2
allele frequency: 1.713032753186241e-5
allele num: 116752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1378G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.228G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3521G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.717G>A
  hgvsp: ENST00000334029.2:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1786G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.717G>A
  hgvsp: ENST00000420436.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1950G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1806G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1041G>A
  hgvsp: ENST00000357068.6:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg347Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

22-18907283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907283
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907283
    reference: chr 22
allele count: 3
allele frequency: 2.572810538231965e-5
allele num: 116604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.716G>A
  hgvsp: ENSP00000410805.1:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3520G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1949G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1040G>A
  hgvsp: ENSP00000349577.6:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1785G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.227G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.716G>A
  hgvsp: ENSP00000334726.2:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1805G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1377G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg347Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

22-18907284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907284
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907284
    reference: chr 22
allele count: 7
allele frequency: 6.017674770468691e-5
allele num: 116324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.715C>T
  hgvsp: ENSP00000410805.1:p.Arg239Trp
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1804C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.715C>T
  hgvsp: ENSP00000334726.2:p.Arg239Trp
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3519C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1784C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1376C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.226C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1039C>T
  hgvsp: ENSP00000349577.6:p.Arg347Trp
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1948C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15140
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg347Trp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-18907305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907305
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907305
    reference: chr 22
allele count: 1
allele frequency: 8.800802633200148e-6
allele num: 113626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.694C>T
  hgvsp: ENSP00000410805.1:p.Gln232Ter
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.694C>T
  hgvsp: ENSP00000334726.2:p.Gln232Ter
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1018C>T
  hgvsp: ENSP00000349577.6:p.Gln340Ter
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1927C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1783C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1355C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.205C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1763C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3498C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3098
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln340Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

22-18907314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907314
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907314
    reference: chr 22
allele count: 11
allele frequency: 9.842343551475457e-5
allele num: 111762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-3C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1774C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-3C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-3C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-3C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-3C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3489C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-3C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1754C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25137
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1012-3C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

22-18907314-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907314
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907314
    reference: chr 22
allele count: 1
allele frequency: 8.947585046795869e-6
allele num: 111762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-3C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-3C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-3C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-3C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-3C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1774C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1754C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-3C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3489C>A
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1012-3C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-18907318-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907318
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907318
    reference: chr 22
allele count: 1
allele frequency: 9.066840750009067e-6
allele num: 110292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1770C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-7C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-7C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-7C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-7C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-7C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1750C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-7C>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3485C>G
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 9.75e1
  variant carriers: 1
hgvs: c.1012-7C>G
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

22-18907320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907320
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907320
    reference: chr 22
allele count: 5
allele frequency: 4.584127915505354e-5
allele num: 109072
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-9C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1748C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-9C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-9C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3483C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-9C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1768C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-9C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-9C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20318
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3096
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12373
  bin: 2.25e1
  variant carriers: 0
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: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

22-18907321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907321
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907321
    reference: chr 22
allele count: 1
allele frequency: 9.169600938967136e-6
allele num: 109056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-10G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-10G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1767G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1747G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3482G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-10G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-10G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-10G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-10G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10833
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-18907326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907326
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907326
    reference: chr 22
allele count: 3
allele frequency: 2.793036030164789e-5
allele num: 107410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-15G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-15G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1762G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-15G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3477G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-15G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-15G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1742G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-15G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11066
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16985
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

22-18907327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907327
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907327
    reference: chr 22
allele count: 7
allele frequency: 6.519754857217368e-5
allele num: 107366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3476C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1761C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1741C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11082
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3098
  bin: 9.75e1
  variant carriers: 7
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

22-18907328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907328
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907328
    reference: chr 22
allele count: 2
allele frequency: 1.86880956830499e-5
allele num: 107020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-17G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-17G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3475G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-17G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-17G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1740G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1760G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-17G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-17G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2935
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

22-18907329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907329
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907329
    reference: chr 22
allele count: 6
allele frequency: 5.63211053955619e-5
allele num: 106532
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-18C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3474C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1739C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-18C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-18C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-18C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-18C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1759C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-18C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15031
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15920
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3287
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23658
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

22-18907329-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907329
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907329
    reference: chr 22
allele count: 1
allele frequency: 9.386850899260316e-6
allele num: 106532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1739C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-18C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3474C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-18C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-18C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-18C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-18C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1759C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-18C>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3287
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-18907330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907330
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907330
    reference: chr 22
allele count: 1
allele frequency: 9.390024038461539e-6
allele num: 106496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-19C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-19C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1738C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-19C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3473C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1758C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-19C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-19C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-19C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15988
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23371
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

22-18907333-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907333
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907333
    reference: chr 22
allele count: 1
allele frequency: 9.495594044363415e-6
allele num: 105312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1755T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3470T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1735T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-22T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-22T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-22T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-22T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-22T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-22T>C
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12900
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3088
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19509
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/22-18907348-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907348
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907348
    reference: chr 22
allele count: 1
allele frequency: 1.010958793319584e-5
allele num: 98916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-37G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3455G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-37G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-37G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-37G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1740G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-37G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1720G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-37G>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19669
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7391
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

22-18907348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907348
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907348
    reference: chr 22
allele count: 77
allele frequency: 7.784382708560799e-4
allele num: 98916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1740G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-37G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-37G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1720G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-37G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-37G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3455G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-37G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-37G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19669
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11756
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5322
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

22-18907349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907349
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907349
    reference: chr 22
allele count: 489
allele frequency: 4.965676916202933e-3
allele num: 98476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-38C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1739C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-38C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-38C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3454C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-38C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-38C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1719C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-38C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 7.5e0
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 1.75e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 2.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19791
  bin: 1.25e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 5271
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7246
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17340
  bin: 2.25e1
  variant carriers: 4
num of homozygotes: 9
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

22-18907350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907350
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907350
    reference: chr 22
allele count: 8
allele frequency: 8.137524158274845e-5
allele num: 98310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1738C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3453C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-39C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-39C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-39C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-39C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-39C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-39C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19839
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

22-18907352-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907352
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907352
    reference: chr 22
allele count: 1
allele frequency: 1.020970738978621e-5
allele num: 97946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-41T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-41T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-41T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3451T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-41T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-41T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1716T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1736T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-41T>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-18907354-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907354
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907354
    reference: chr 22
allele count: 1
allele frequency: 1.028298782494242e-5
allele num: 97248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1714T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-43T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1734T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-43T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-43T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3449T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-43T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-43T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-43T>G
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1558
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5479
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

22-18907355-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907355
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907355
    reference: chr 22
allele count: 2
allele frequency: 2.098151528503388e-5
allele num: 95322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1733C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3448C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-44C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-44C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-44C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-44C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-44C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1713C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-44C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5433
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

22-18907359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18907359
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18907359
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 92394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.199-48G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.1709G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.688-48G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.1729G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.688-48G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1012-48G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.3444G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1349-48G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1921-48G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5590
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

22-18908809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908809
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908809
    reference: chr 22
allele count: 72
allele frequency: 3.428244929054376e-3
allele num: 21002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.279C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+46C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+46C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.259C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1994C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+46C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+46C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+46C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+46C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31964
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

22-18908814-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908814
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908814
    reference: chr 22
allele count: 1
allele frequency: 4.76009139375476e-5
allele num: 21008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+41C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.274C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+41C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+41C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+41C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+41C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.254C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+41C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1989C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32381
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

22-18908814-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908814
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908814
    reference: chr 22
allele count: 1
allele frequency: 4.76009139375476e-5
allele num: 21008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.274C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.254C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+41C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1989C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+41C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+41C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+41C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+41C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+41C>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/22-18908816-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908816
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908816
    reference: chr 22
allele count: 1
allele frequency: 4.75873227372228e-5
allele num: 21014
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+39G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.272G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+39G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+39G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.252G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1987G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+39G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+39G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+39G>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25908
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7452
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

22-18908826-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908826
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908827
    reference: chr 22
allele count: 27
allele frequency: 1.282660332541568e-3
allele num: 21050
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+28dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+28dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.241dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+28dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1976dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+28dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+28dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.261dupC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+28dupC
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 32965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3910
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2800
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

22-18908833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908833
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908833
    reference: chr 22
allele count: 6
allele frequency: 2.840102243680772e-4
allele num: 21126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+22G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+22G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.235G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+22G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+22G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+22G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+22G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.255G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1970G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3791
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

22-18908839-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908839
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908839
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 21192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.229C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.249C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1964C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+16C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+16C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32951
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7459
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29962
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ

22-18908843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908843
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908843
    reference: chr 22
allele count: 1
allele frequency: 4.709428275407365e-5
allele num: 21234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.245G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1960G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+12G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.225G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+12G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+12G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+12G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+12G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+12G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

22-18908844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908844
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908844
    reference: chr 22
allele count: 2
allele frequency: 9.414422895876483e-5
allele num: 21244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1959C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.244C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.198+11C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1348+11C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1920+11C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.687+11C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.687+11C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1011+11C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.224C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5688
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

22-18908864-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908864
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908864
    reference: chr 22
allele count: 2
allele frequency: 9.18526683200147e-5
allele num: 21774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.189C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1939C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.224C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.678C>T
  hgvsp: ENST00000334029.2:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.1002C>T
  hgvsp: ENST00000357068.6:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1339C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.678C>T
  hgvsp: ENST00000420436.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.204C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1911C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30405
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7708
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7461
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro334Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

22-18908867-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908867
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908866
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 21876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1907delT
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1335delT
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.220delT
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.200delT
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.674delT
  hgvsp: ENSP00000410805.1:p.Val225AlafsTer24
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.998delT
  hgvsp: ENSP00000349577.6:p.Val333AlafsTer24
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1935delT
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.674delT
  hgvsp: ENSP00000334726.2:p.Val225AlafsTer24
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.185delT
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30089
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28946
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val333AlafsTer24
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: GA
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/22-18908874-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908874
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908874
    reference: chr 22
allele count: 1
allele frequency: 4.525296406914653e-5
allele num: 22098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1329T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1929T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.668T>G
  hgvsp: ENSP00000334726.2:p.Leu223Trp
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.668T>G
  hgvsp: ENSP00000410805.1:p.Leu223Trp
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.179T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.194T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1901T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.214T>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.992T>G
  hgvsp: ENSP00000349577.6:p.Leu331Trp
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28874
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27816
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu331Trp
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

22-18908875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908875
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908875
    reference: chr 22
allele count: 17623
allele frequency: 6.781206710789596e-1
allele num: 25988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1328T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.193T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.178T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1900T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.667T>C
  hgvsp: ENST00000420436.1:c.667T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1928T>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.667T>C
  hgvsp: ENST00000334029.2:c.667T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.991T>C
  hgvsp: ENST00000357068.6:c.991T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.213T>C
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.25e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 1.25e1
  variant carriers: 2205
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 281
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.25e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 346
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.75e1
  variant carriers: 347
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 329
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 16705
  bin: 2.5e0
  variant carriers: 6713
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 222
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 352
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 7.5e0
  variant carriers: 10583
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 9.75e1
  variant carriers: 5206
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.25e1
  variant carriers: 282
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 6.25e1
  variant carriers: 612
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 3.25e1
  variant carriers: 910
genotype quality: GenotypeQuality
  all individuals: 10400
  bin: 7.5e0
  variant carriers: 3361
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 1.25e1
  variant carriers: 2766
genotype quality: GenotypeQuality
  all individuals: 3927
  bin: 2.25e1
  variant carriers: 2308
hgvs: p.Leu331Leu
num of homozygotes: 5871
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

22-18908879-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908879
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908879
    reference: chr 22
allele count: 1
allele frequency: 4.392515154177282e-5
allele num: 22766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.663G>C
  hgvsp: ENSP00000410805.1:p.Lys221Asn
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.174G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1924G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1324G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.987G>C
  hgvsp: ENSP00000349577.6:p.Lys329Asn
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.663G>C
  hgvsp: ENSP00000334726.2:p.Lys221Asn
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1896G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.189G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.209G>C
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys329Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

22-18908932-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908932
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908932
    reference: chr 22
allele count: 5
allele frequency: 2.414059482425647e-4
allele num: 20712
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.934A>G
  hgvsp: ENSP00000349577.6:p.Met312Val
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.610A>G
  hgvsp: ENSP00000410805.1:p.Met204Val
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1871A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.121A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.136A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1271A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1843A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.515A>G
  hgvsp: ENSP00000409742.1:p.Met173Val
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.610A>G
  hgvsp: ENSP00000334726.2:p.Met204Val
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.156A>G
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30565
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2377
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Met312Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

22-18908933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908933
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908933
    reference: chr 22
allele count: 4
allele frequency: 1.936670862786869e-4
allele num: 20654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.135C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.609C>T
  hgvsp: ENST00000334029.2:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1842C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.933C>T
  hgvsp: ENST00000357068.6:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1870C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.609C>T
  hgvsp: ENST00000420436.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.155C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1270C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.514C>T
  hgvsp: ENST00000438924.1:c.514C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.120C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30239
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Thr311Thr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

22-18908937-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908937
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908937
    reference: chr 22
allele count: 5
allele frequency: 2.429779376032656e-4
allele num: 20578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.606-1G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.511-1G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.606-1G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.930-1G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.116G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1267-1G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1838G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1866G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.131G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.151G>C
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: c.930-1G>C
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

22-18908943-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908943
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908943
    reference: chr 22
allele count: 1
allele frequency: 4.900039200313603e-5
allele num: 20408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.606-7C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.606-7C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.511-7C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.930-7C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.125C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1832C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1860C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1267-7C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.110C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.145C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
hgvs: c.930-7C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

22-18908951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908951
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908951
    reference: chr 22
allele count: 125
allele frequency: 6.211488769628305e-3
allele num: 20124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.511-15C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.606-15C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.930-15C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1824C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1267-15C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.117C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1852C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.137C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.102C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.606-15C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 26327
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3145
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS

22-18908958-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908958
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908958
    reference: chr 22
allele count: 1
allele frequency: 4.987033712347896e-5
allele num: 20052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1817G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.606-22G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.95G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.110G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.130G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1845G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.930-22G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.511-22G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1267-22G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.606-22G>C
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

22-18908961-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18908961
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18908960
    reference: chr 22
allele count: 3
allele frequency: 1.497902935889754e-4
allele num: 20028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1841delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.511-26delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000313755
  gene symbol: PRODH
  hgvsc: ENST00000313755.5:n.126delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000446371
  gene symbol: PRODH
  hgvsc: ENST00000446371.1:n.91delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.930-26delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.606-26delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000609229
  gene symbol: PRODH
  hgvsc: ENST00000609229.1:n.106delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.606-26delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1267-26delC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.1813delC
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: AG
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

22-18909793-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909793
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909793
    reference: chr 22
allele count: 1
allele frequency: 1.947343823025393e-5
allele num: 51352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.982G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.1010G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+45G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+45G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+45G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+45G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+45G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.438G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6267
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

22-18909805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909805
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909805
    reference: chr 22
allele count: 10
allele frequency: 1.886934863008529e-4
allele num: 52996
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+33G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+33G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.998G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+33G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.426G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.970G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+33G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+33G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13967
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26147
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2021
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7328
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

22-18909807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909807
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909807
    reference: chr 22
allele count: 1
allele frequency: 1.868390568364411e-5
allele num: 53522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.424G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+31G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+31G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.968G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+31G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.996G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+31G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+31G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14024
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6722
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-18909808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909808
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909808
    reference: chr 22
allele count: 278
allele frequency: 5.121591746499631e-3
allele num: 54280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+30C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+30C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.423C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.967C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+30C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.995C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+30C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+30C>T
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26591
  bin: 7.5e0
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 1.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 13890
  bin: 1.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 4.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6145
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 4611
  bin: 3.25e1
  variant carriers: 2
num of homozygotes: 3
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

22-18909808-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909808
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909808
    reference: chr 22
allele count: 10
allele frequency: 1.842299189388357e-4
allele num: 54280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+30C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.423C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+30C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+30C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+30C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.995C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.967C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+30C>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26591
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13890
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26682
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4611
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff

22-18909812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909812
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909812
    reference: chr 22
allele count: 1
allele frequency: 1.778599886169607e-5
allele num: 56224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+26G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.963G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+26G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+26G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+26G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.991G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.419G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+26G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 13483
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4548
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

22-18909832-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909832
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909832
    reference: chr 22
allele count: 1
allele frequency: 1.312921776120579e-5
allele num: 76166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.971A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+6A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+6A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.943A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+6A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.399A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+6A>G
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+6A>G
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
hgvs: c.929+6A>G
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

22-18909835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909835
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909835
    reference: chr 22
allele count: 6
allele frequency: 7.410517995207865e-5
allele num: 80966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.396G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1266+3G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.929+3G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.968G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.605+3G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.510+3G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.605+3G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.940G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21999
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 2.75e1
  variant carriers: 0
hgvs: c.929+3G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS

22-18909843-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909843
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909843
    reference: chr 22
allele count: 1
allele frequency: 1.058357851956904e-5
allele num: 94486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.505G>C
  hgvsp: ENST00000438924.1:c.505G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.924G>C
  hgvsp: ENST00000357068.6:c.924G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.600G>C
  hgvsp: ENST00000334029.2:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.960G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.932G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.600G>C
  hgvsp: ENST00000420436.1:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1261G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.388G>C
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30402
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val308Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

22-18909847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909847
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909847
    reference: chr 22
allele count: 4
allele frequency: 3.973694144761678e-5
allele num: 100662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.596G>A
  hgvsp: ENSP00000410805.1:p.Gly199Glu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.920G>A
  hgvsp: ENSP00000349577.6:p.Gly307Glu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.596G>A
  hgvsp: ENSP00000334726.2:p.Gly199Glu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.384G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.928G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.956G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1257G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.501G>A
  hgvsp: ENSP00000409742.1:p.Gly168Glu
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33246
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly307Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

22-18909849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909849
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909849
    reference: chr 22
allele count: 5
allele frequency: 4.832785617630002e-5
allele num: 103460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.594G>A
  hgvsp: ENST00000420436.1:c.594G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.954G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.499G>A
  hgvsp: ENST00000438924.1:c.499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.594G>A
  hgvsp: ENST00000334029.2:c.594G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.918G>A
  hgvsp: ENST00000357068.6:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.382G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1255G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.926G>A
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34862
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu306Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

22-18909852-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909852
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909852
    reference: chr 22
allele count: 1
allele frequency: 9.366277653934773e-6
allele num: 106766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.951C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.496C>T
  hgvsp: ENST00000438924.1:c.496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.923C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.379C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.591C>T
  hgvsp: ENST00000420436.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.915C>T
  hgvsp: ENST00000357068.6:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1252C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.591C>T
  hgvsp: ENST00000334029.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36418
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr305Thr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-18909862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909862
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909862
    reference: chr 22
allele count: 2
allele frequency: 1.75377060680463e-5
allele num: 114040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.581C>T
  hgvsp: ENSP00000410805.1:p.Thr194Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.581C>T
  hgvsp: ENSP00000334726.2:p.Thr194Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1242C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.369C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.913C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.941C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.486C>T
  hgvsp: ENSP00000409742.1:p.Thr163Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.905C>T
  hgvsp: ENSP00000349577.6:p.Thr302Met
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6313
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr302Met
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

22-18909864-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909864
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909864
    reference: chr 22
allele count: 1
allele frequency: 8.690966609306287e-6
allele num: 115062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1240C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.911C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.484C>A
  hgvsp: ENSP00000409742.1:p.Phe162Leu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.579C>A
  hgvsp: ENSP00000410805.1:p.Phe193Leu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.939C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.903C>A
  hgvsp: ENSP00000349577.6:p.Phe301Leu
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.367C>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.579C>A
  hgvsp: ENSP00000334726.2:p.Phe193Leu
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe301Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

22-18909868-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909868
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909868
    reference: chr 22
allele count: 1
allele frequency: 8.589294303580018e-6
allele num: 116424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.935G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.363G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.480G>C
  hgvsp: ENSP00000409742.1:p.Trp161Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.575G>C
  hgvsp: ENSP00000410805.1:p.Trp192Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.907G>C
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.899G>C
  hgvsp: ENSP00000349577.6:p.Trp300Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.575G>C
  hgvsp: ENSP00000334726.2:p.Trp192Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1236G>C
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Trp300Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/22-18909872-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909872
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909872
    reference: chr 22
allele count: 2
allele frequency: 1.706746769981738e-5
allele num: 117182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.571G>T
  hgvsp: ENSP00000334726.2:p.Asp191Tyr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.931G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.903G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.359G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.476G>T
  hgvsp: ENSP00000409742.1:p.Asp160Tyr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1232G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.895G>T
  hgvsp: ENSP00000349577.6:p.Asp299Tyr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.571G>T
  hgvsp: ENSP00000410805.1:p.Asp191Tyr
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp299Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

22-18909884-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909884
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909884
    reference: chr 22
allele count: 1
allele frequency: 8.429570934839416e-6
allele num: 118630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.919G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.559G>A
  hgvsp: ENSP00000334726.2:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1220G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.347G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.883G>A
  hgvsp: ENSP00000349577.6:p.Ala295Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.891G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.464G>A
  hgvsp: ENSP00000409742.1:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.559G>A
  hgvsp: ENSP00000410805.1:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41303
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala295Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

22-18909887-T-TGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909887
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909889
    reference: chr 22
allele count: 1
allele frequency: 8.417508417508417e-6
allele num: 118800
alternate allele: TGG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.459_460dupCC
  hgvsp: ENSP00000409742.1:p.Arg155ProfsTer?
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.914_915dupCC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1215_1216dupCC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000396806
  ensembl transcript: ENST00000450579
  gene symbol: PRODH
  hgvsc: ENST00000450579.1:c.401_402dupCC
  hgvsp: ENSP00000396806.1:p.Arg135ProfsTer?
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.554_555dupCC
  hgvsp: ENSP00000334726.2:p.Arg186ProfsTer40
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.554_555dupCC
  hgvsp: ENSP00000410805.1:p.Arg186ProfsTer40
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.878_879dupCC
  hgvsp: ENSP00000349577.6:p.Arg294ProfsTer40
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.886_887dupCC
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.342_343dupCC
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3429
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg294ProfsTer40
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

22-18909893-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909893
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909893
    reference: chr 22
allele count: 1
allele frequency: 8.396164631996104e-6
allele num: 119102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.882G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.338G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.455G>A
  hgvsp: ENSP00000409742.1:p.Ala153Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.550G>A
  hgvsp: ENSP00000334726.2:p.Ala184Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000396806
  ensembl transcript: ENST00000450579
  gene symbol: PRODH
  hgvsc: ENST00000450579.1:c.397G>A
  hgvsp: ENSP00000396806.1:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.874G>A
  hgvsp: ENSP00000349577.6:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.910G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1211G>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.550G>A
  hgvsp: ENSP00000410805.1:p.Ala184Thr
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41117
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6314
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala292Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

22-18909894-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909894
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909894
    reference: chr 22
allele count: 9
allele frequency: 7.549955539150713e-5
allele num: 119206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.549C>T
  hgvsp: ENST00000334029.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.549C>T
  hgvsp: ENST00000420436.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1210C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.881C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.337C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.454C>T
  hgvsp: ENST00000438924.1:c.454C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.873C>T
  hgvsp: ENST00000357068.6:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.909C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000396806
  ensembl transcript: ENST00000450579
  gene symbol: PRODH
  hgvsc: ENST00000450579.1:c.396C>T
  hgvsp: ENST00000450579.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41148
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8853
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile291Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

22-18909902-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909902
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909902
    reference: chr 22
allele count: 498
allele frequency: 4.186492257511307e-3
allele num: 118954
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.329T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1202T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.541T>A
  hgvsp: ENSP00000410805.1:p.Leu181Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000396806
  ensembl transcript: ENST00000450579
  gene symbol: PRODH
  hgvsc: ENST00000450579.1:c.388T>A
  hgvsp: ENSP00000396806.1:p.Leu130Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.901T>A
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.541T>A
  hgvsp: ENSP00000334726.2:p.Leu181Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.446T>A
  hgvsp: ENSP00000409742.1:p.Leu150Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  clinical significance: pathogenic&risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.865T>A
  hgvsp: ENSP00000349577.6:p.Leu289Met
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  clinical significance: pathogenic&risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.873T>A
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 2.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 40073
  bin: 2.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 3.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 3.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 7.75e1
  variant carriers: 11
hgvs: p.Leu289Met
num of homozygotes: 2
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/22-18909908-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909908
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909908
    reference: chr 22
allele count: 2
allele frequency: 1.68084176555619e-5
allele num: 118988
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.859G>T
  hgvsp: ENSP00000349577.6:p.Ala287Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.440G>T
  hgvsp: ENSP00000409742.1:p.Ala148Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.323G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.867G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000396806
  ensembl transcript: ENST00000450579
  gene symbol: PRODH
  hgvsc: ENST00000450579.1:c.382G>T
  hgvsp: ENSP00000396806.1:p.Ala128Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1196G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.895G>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.535G>T
  hgvsp: ENSP00000334726.2:p.Ala179Ser
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.535G>T
  hgvsp: ENSP00000410805.1:p.Ala179Ser
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9254
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala287Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-18909909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18909909
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 18909909
    reference: chr 22
allele count: 2
allele frequency: 1.680813513740651e-5
allele num: 118990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000409742
  ensembl transcript: ENST00000438924
  gene symbol: PRODH
  hgvsc: ENST00000438924.1:c.439C>T
  hgvsp: ENST00000438924.1:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000410805
  ensembl transcript: ENST00000420436
  gene symbol: PRODH
  hgvsc: ENST00000420436.1:c.534C>T
  hgvsp: ENST00000420436.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000429300
  gene symbol: PRODH
  hgvsc: ENST00000429300.1:n.1195C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000491604
  gene symbol: PRODH
  hgvsc: ENST00000491604.1:n.866C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000399694
  gene symbol: PRODH
  hgvsc: ENST00000399694.1:n.322C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000334726
  ensembl transcript: ENST00000334029
  gene symbol: PRODH
  hgvsc: ENST00000334029.2:c.534C>T
  hgvsp: ENST00000334029.2:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100033
  ensembl transcript: ENST00000482858
  gene symbol: PRODH
  hgvsc: ENST00000482858.1:n.894C>T
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000396806
  ensembl transcript: ENST00000450579
  gene symbol: PRODH
  hgvsc: ENST00000450579.1:c.381C>T
  hgvsp: ENST00000450579.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100033
  ensembl protein: ENSP00000349577
  ensembl transcript: ENST00000357068
  gene symbol: PRODH
  hgvsc: ENST00000357068.6:c.858C>T
  hgvsp: ENST00000357068.6:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9453
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9309
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val286Val
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 3104
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 855
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3081
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4382
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.095112816862175e-5
allele num: 64618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11138
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.528502e6

MQRankSum
type: SiteQuality
SIO_000300: -1.235e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.754e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.018e0

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.805e0

VQSLOD
type: SiteQuality
SIO_000300: -6.28e-1

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 210
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 440
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11128
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.00928542591845e-4
allele num: 9908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

DP
type: SiteQuality
SIO_000300: 1.525555e6

VQSLOD
type: SiteQuality
SIO_000300: -2.195e0

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.6347e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

GenotypeQuality
all individuals: 204
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11110
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.009896990506968e-4
allele num: 9902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550051151688006e-5
allele num: 64514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15544
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.87e-1

FS
type: SiteQuality
SIO_000300: 6.394e0

VQSLOD
type: SiteQuality
SIO_000300: -1.14e0

QD
type: SiteQuality
SIO_000300: 8.699999999999999e0

DP
type: SiteQuality
SIO_000300: 1.524479e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.291e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.9e1

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4341
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3103
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 413
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43199
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.103565997330933e-5
allele num: 64442
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.185114956150747e-4
allele num: 8438
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.374000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.523314e6

MQ
type: SiteQuality
SIO_000300: 5.796e1

FS
type: SiteQuality
SIO_000300: 1.229e0

QD
type: SiteQuality
SIO_000300: 2.585e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

GenotypeQuality
all individuals: 3742
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4266
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.187648456057007e-4
allele num: 8420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.111581305619516e-5
allele num: 64276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.583311805734952e-4
allele num: 15484
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

FS
type: SiteQuality
SIO_000300: 2.13e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 7.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

DP
type: SiteQuality
SIO_000300: 1.517619e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 468
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6752
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38645
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588663298700473e-5
allele num: 62946
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.454e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.113e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.464593e6

QD
type: SiteQuality
SIO_000300: 8.94e0

GenotypeQuality
all individuals: 803
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1427
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.919385796545106e-4
allele num: 10420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.453065969195002e-4
allele num: 61938
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

QD
type: SiteQuality
SIO_000300: 1.125e1

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

DP
type: SiteQuality
SIO_000300: 1.425944e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

FS
type: SiteQuality
SIO_000300: 3.151e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 3619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 708
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.614517743550002e-5
allele num: 61938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.125e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 1.425944e6

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 3.151e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

GenotypeQuality
all individuals: 10879
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3434
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9472
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.742179072276159e-5
allele num: 14832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61132
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.360000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
type: SiteQuality
SIO_000300: 1.536e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.324e0

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

DP
type: SiteQuality
SIO_000300: 1.386564e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60402
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.396277679663089e-4
allele num: 14722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.353711e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

FS
type: SiteQuality
SIO_000300: 7.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.564e0

QD
type: SiteQuality
SIO_000300: 1.107e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.786102062975027e-5
allele num: 14736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.32e1

VQSLOD
type: SiteQuality
SIO_000300: -1.212e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.821e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 1.353164e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
SIO_000300: 3.522e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.89e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.681124335955887e-5
allele num: 59484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5642
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.017293997965412e-4
allele num: 9830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7776
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.074113856068743e-4
allele num: 9310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

DP
type: SiteQuality
SIO_000300: 1.29584e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.3e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

FS
type: SiteQuality
SIO_000300: 3.185e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1028
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5650
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.450225757901526e-4
allele num: 9302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59452
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.01667344448963e-4
allele num: 9836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.283e1

MQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

DP
type: SiteQuality
SIO_000300: 1.294597e6

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.123e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.55e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5624
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.374502260916515e-5
allele num: 59268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.295e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 1.284657e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 262
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.029018316526034e-4
allele num: 9718
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.163097555699762e-4
allele num: 9246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14472
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.390405153415834e-5
allele num: 58990
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.786352268667381e-4
allele num: 5598
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.703e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.021e0

VQSLOD
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

DP
type: SiteQuality
SIO_000300: 1.275983e6

MQ
type: SiteQuality
SIO_000300: 5.893e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.909894969596462e-5
allele num: 14472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.82e-1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.175e1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 784
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.029866117404737e-4
allele num: 9710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58990
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14468
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQ
type: SiteQuality
SIO_000300: 5.85e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

FS
type: SiteQuality
SIO_000300: 1.882e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e0

QD
type: SiteQuality
SIO_000300: 1.195e1

VQSLOD
type: SiteQuality
SIO_000300: -1.596e0

DP
type: SiteQuality
SIO_000300: 1.266417e6

GenotypeQuality
all individuals: 17044
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9148
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.712152861007431e-5
allele num: 58406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

DP
type: SiteQuality
SIO_000300: 1.223932e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

QD
type: SiteQuality
SIO_000300: 1.198e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.821095571095571e-5
allele num: 54912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.143e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

QD
type: SiteQuality
SIO_000300: 1.342e1

DP
type: SiteQuality
SIO_000300: 1.096458e6

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3152
bin: 9.75e1
variant carriers: 72

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.152870647913304e-4
allele num: 8674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.329399766899767e-3
allele num: 54912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13660
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.445107946715664e-4
allele num: 8708
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.342e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

FS
type: SiteQuality
SIO_000300: 1.143e0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.096458e6

GenotypeQuality
all individuals: 2027
bin: 7.5e0
variant carriers: 3

GenotypeQuality
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variant carriers: 468

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

GenotypeQuality
all individuals: 444
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variant carriers: 3

GenotypeQuality
all individuals: 8919
bin: 6.25e1
variant carriers: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7106
num of homozygotes: 0

Latino
type: Population
allele count: 479
allele frequency: 5.623385771307818e-2
allele num: 8518
num of homozygotes: 9

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5080
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.315021396437584e-5
allele num: 54682
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.883891693437356e-4
allele num: 8716
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.14e0

QD
type: SiteQuality
SIO_000300: 1.527e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.093831e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.281628767073126e-4
allele num: 54618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.148369315571888e-4
allele num: 8708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

FS
type: SiteQuality
SIO_000300: 1.207e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

DP
type: SiteQuality
SIO_000300: 1.087649e6

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

QD
type: SiteQuality
SIO_000300: 1.242e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.83749219065819e-5
allele num: 54422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 1.078173e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.263e0

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

QD
type: SiteQuality
SIO_000300: 1.342e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.203948952564411e-4
allele num: 8306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54056
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

MQ
type: SiteQuality
SIO_000300: 5.845e1

DP
type: SiteQuality
SIO_000300: 1.071781e6

QD
type: SiteQuality
SIO_000300: 5.24e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 889
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GenotypeQuality
all individuals: 2434
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6892
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.474958887726118e-5
allele num: 13378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.887647236484446e-5
allele num: 52976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.027e1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 1.064312e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 4247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13477
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5383
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3073
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2970
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13158
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

DP
type: SiteQuality
SIO_000300: 1.056132e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.221e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

QD
type: SiteQuality
SIO_000300: 7.84e0

VQSLOD
type: SiteQuality
SIO_000300: -1.337e0

GenotypeQuality
all individuals: 1187
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7471
bin: 9.75e1
variant carriers: 67

GenotypeQuality
all individuals: 899
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 8657
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 185
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 21956
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.233139794551139e-4
allele num: 8956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 67
allele frequency: 2.384341637010676e-2
allele num: 2810
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.439024390243902e-3
allele num: 410
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506024096385542e-3
allele num: 664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.263902932254803e-4
allele num: 7912
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.682e1

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

DP
type: SiteQuality
SIO_000300: 6.79531e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.76e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7451
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24630
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6542
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.263902932254803e-4
allele num: 7912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.85027e5

VQSLOD
type: SiteQuality
SIO_000300: -1.136e0

FS
type: SiteQuality
SIO_000300: 7.359e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6542
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7451
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.55366027007818e-4
allele num: 2814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.359e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

VQSLOD
type: SiteQuality
SIO_000300: -1.136e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 6.85027e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
all individuals: 5524
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.050505050505051e-3
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 6.87691e5

QD
type: SiteQuality
SIO_000300: 1.244e1

VQSLOD
type: SiteQuality
SIO_000300: -9.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.8e-1

FS
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 5.85e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.82e-2

GenotypeQuality
all individuals: 1033
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7461
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 3.003337041156841e-3
allele num: 8990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2822
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.185e0

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.85e-1

MQ
type: SiteQuality
SIO_000300: 5.579e1

QD
type: SiteQuality
SIO_000300: 1.061e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 6.9907e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.26e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

GenotypeQuality
all individuals: 193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29386
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7459
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2828
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.579585649317837e-4
allele num: 7916
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 7.08008e5

FS
type: SiteQuality
SIO_000300: 4.281e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.04e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.068e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

MQ
type: SiteQuality
SIO_000300: 5.682e1

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.12e0

MQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 7.15411e5

VQSLOD
type: SiteQuality
SIO_000300: -3.048e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.573e1

GenotypeQuality
all individuals: 2136
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7459
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.528581510232887e-4
allele num: 2834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.78e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

DP
type: SiteQuality
SIO_000300: 7.20486e5

FS
type: SiteQuality
SIO_000300: 6.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.853e1

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 804
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7460
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 194
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.262945188178833e-4
allele num: 7918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.408450704225352e-3
allele num: 710
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.608e-1

MQ
type: SiteQuality
SIO_000300: 5.833e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.73e-2

DP
type: SiteQuality
SIO_000300: 7.23172e5

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

FS
type: SiteQuality
SIO_000300: 6.516e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29193
bin: 7.5e0
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.439024390243902e-3
allele num: 820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.45023e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.007e-1

MQ
type: SiteQuality
SIO_000300: 5.37e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 4.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.06e-2

GenotypeQuality
all individuals: 197
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7685
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 313
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2918
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.94e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 7.46809e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.573e1

GenotypeQuality
all individuals: 7200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1370
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7463
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variant carriers: 1

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
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GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
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GenotypeQuality
all individuals: 2872
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.04384133611691e-4
allele num: 9580
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.656e0

MQRankSum
type: SiteQuality
SIO_000300: -8.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.553e0

VQSLOD
type: SiteQuality
SIO_000300: -1.36e0

DP
type: SiteQuality
SIO_000300: 7.5169e5

FS
type: SiteQuality
SIO_000300: 5.058e0

MQ
type: SiteQuality
SIO_000300: 5.768e1

QD
type: SiteQuality
SIO_000300: 2.342e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.61e-2

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 219

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 96

GenotypeQuality
all individuals: 6540
bin: 2.5e0
variant carriers: 20

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 163

GenotypeQuality
all individuals: 4112
bin: 1.75e1
variant carriers: 3939

GenotypeQuality
all individuals: 431
bin: 5.75e1
variant carriers: 429

GenotypeQuality
all individuals: 211
bin: 8.25e1
variant carriers: 145

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 213

GenotypeQuality
all individuals: 389
bin: 7.25e1
variant carriers: 343

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 167

GenotypeQuality
all individuals: 286
bin: 3.75e1
variant carriers: 278

GenotypeQuality
all individuals: 11236
bin: 9.75e1
variant carriers: 10915

GenotypeQuality
all individuals: 1180
bin: 2.75e1
variant carriers: 1167

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 423

GenotypeQuality
all individuals: 757
bin: 6.75e1
variant carriers: 620

African
type: Population
allele count: 2884
allele frequency: 8.273092369477911e-1
allele num: 3486
num of homozygotes: 1178

Latino
type: Population
allele count: 340
allele frequency: 6.007067137809188e-1
allele num: 566
num of homozygotes: 98

South Asian
type: Population
allele count: 5707
allele frequency: 6.952972709551657e-1
allele num: 8208
num of homozygotes: 2009

European (Finnish)
type: Population
allele count: 130
allele frequency: 5.963302752293578e-1
allele num: 218
num of homozygotes: 31

East Asian
type: Population
allele count: 1187
allele frequency: 8.063858695652174e-1
allele num: 1472
num of homozygotes: 467

European (Non-Finnish)
type: Population
allele count: 7251
allele frequency: 6.128296146044625e-1
allele num: 11832
num of homozygotes: 2051

Other
type: Population
allele count: 124
allele frequency: 6.019417475728155e-1
allele num: 206
num of homozygotes: 37

MQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.36e1

DP
type: SiteQuality
SIO_000300: 1.282381e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.728e-1

MQ
type: SiteQuality
SIO_000300: 5.619e1

VQSLOD
type: SiteQuality
SIO_000300: 8.699999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
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variant carriers: 0

GenotypeQuality
all individuals: 1652
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GenotypeQuality
all individuals: 6355
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GenotypeQuality
all individuals: 1281
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GenotypeQuality
all individuals: 2462
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GenotypeQuality
all individuals: 665
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GenotypeQuality
all individuals: 3749
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variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.251877816725087e-4
allele num: 7988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 974
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.42865e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.477e-1

QD
type: SiteQuality
SIO_000300: 5.16e0

FS
type: SiteQuality
SIO_000300: 1.114e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.508e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.15e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

MQ
type: SiteQuality
SIO_000300: 5.513e1

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

GenotypeQuality
all individuals: 1152
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
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GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 697
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 381
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GenotypeQuality
all individuals: 28954
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 281
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GenotypeQuality
all individuals: 440
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GenotypeQuality
all individuals: 507
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GenotypeQuality
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GenotypeQuality
all individuals: 3534
bin: 6.25e1
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GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 4.597701149425287e-4
allele num: 8700
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.62844702467344e-4
allele num: 2756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.413e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.88e-1

MQ
type: SiteQuality
SIO_000300: 5.756e1

DP
type: SiteQuality
SIO_000300: 4.74103e5

QD
type: SiteQuality
SIO_000300: 1.056e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.52e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

FS
type: SiteQuality
SIO_000300: 1.363e0

GenotypeQuality
all individuals: 2209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
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GenotypeQuality
all individuals: 1138
bin: 6.75e1
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GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 507
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GenotypeQuality
all individuals: 28532
bin: 7.5e0
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GenotypeQuality
all individuals: 128
bin: 2.75e1
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 365
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GenotypeQuality
all individuals: 338
bin: 1.75e1
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GenotypeQuality
all individuals: 2036
bin: 2.5e0
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GenotypeQuality
all individuals: 3467
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 4.616805170821791e-4
allele num: 8664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.71301e5

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.604e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 1.587e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.56e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.069e1

GenotypeQuality
all individuals: 2009
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28191
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 5.807200929152149e-4
allele num: 8610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 4.66839e5

FS
type: SiteQuality
SIO_000300: 5.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.781e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2409
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2440
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.263264274886306e-4
allele num: 7916
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.885e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.59e-2

DP
type: SiteQuality
SIO_000300: 4.54881e5

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.957e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.187e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 175
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 997
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23522
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 226
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 251
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 502
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2814
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2468
bin: 9.75e1
variant carriers: 89

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 404
bin: 7.25e1
variant carriers: 2

South Asian
type: Population
allele count: 25
allele frequency: 3.164556962025316e-3
allele num: 7900
num of homozygotes: 1

African
type: Population
allele count: 43
allele frequency: 1.603281133482476e-2
allele num: 2682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.208333333333333e-3
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 6.745362563237774e-3
allele num: 8302
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.45e-2

DP
type: SiteQuality
SIO_000300: 4.38576e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.924e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 8.210000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -1.104e0

MQ
type: SiteQuality
SIO_000300: 5.767e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.003e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20613
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 262
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 307
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.212121212121212e-4
allele num: 8250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 1.3497e1

VQSLOD
type: SiteQuality
SIO_000300: -1.736e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.46e-2

QD
type: SiteQuality
SIO_000300: 1.44e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.2109e5

GenotypeQuality
all individuals: 2388
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.794586390083481e-4
allele num: 7906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2662
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.405e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

VQSLOD
type: SiteQuality
SIO_000300: -8.310999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 1.1975e1

DP
type: SiteQuality
SIO_000300: 4.18301e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.51e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

GenotypeQuality
all individuals: 317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8725
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4705
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5340
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4220
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.723840023832576e-5
allele num: 26854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3450
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.794e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.13e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

DP
type: SiteQuality
SIO_000300: 9.02447e5

MQ
type: SiteQuality
SIO_000300: 2.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

GenotypeQuality
all individuals: 346
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1961
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2929
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4772
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6276
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 2
allele frequency: 4.739336492890995e-4
allele num: 4220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.013693113169553e-4
allele num: 4966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 2.519435646415203e-4
allele num: 27784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10538
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.276e0

MQ
type: SiteQuality
SIO_000300: 2.854e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 9.24177e5

VQSLOD
type: SiteQuality
SIO_000300: -4.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 4.268e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4705
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4424
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25889
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1951
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5020
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.558718861209964e-5
allele num: 28100
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

DP
type: SiteQuality
SIO_000300: 9.34389e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.681e0

MQ
type: SiteQuality
SIO_000300: 2.96e1

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.078e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.625e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 9

GenotypeQuality
all individuals: 673
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26682
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 563
bin: 6.75e1
variant carriers: 11

GenotypeQuality
all individuals: 321
bin: 7.25e1
variant carriers: 14

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3016
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 9

GenotypeQuality
all individuals: 339
bin: 8.25e1
variant carriers: 10

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 6473
bin: 9.75e1
variant carriers: 221

African
type: Population
allele count: 248
allele frequency: 4.798761609907121e-2
allele num: 5168
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 5.62311098615309e-4
allele num: 28454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1542
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 2.968036529680365e-3
allele num: 4380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3734
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.42151874882231e-5
allele num: 10614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

QD
type: SiteQuality
SIO_000300: 1.135e1

FS
type: SiteQuality
SIO_000300: 2.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.405e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

DP
type: SiteQuality
SIO_000300: 9.45578e5

MQ
type: SiteQuality
SIO_000300: 2.897e1

GenotypeQuality
all individuals: 321
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6473
bin: 9.75e1
variant carriers: 8

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 3.514444366345681e-4
allele num: 28454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

MQ
type: SiteQuality
SIO_000300: 2.897e1

QD
type: SiteQuality
SIO_000300: 1.135e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.405e0

FS
type: SiteQuality
SIO_000300: 2.0e1

DP
type: SiteQuality
SIO_000300: 9.45578e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1168
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.87336080929187e-4
allele num: 5338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.304e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

MQ
type: SiteQuality
SIO_000300: 2.629e1

FS
type: SiteQuality
SIO_000300: 3.358e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 9.70893e5

QD
type: SiteQuality
SIO_000300: 7.83e0

GenotypeQuality
all individuals: 388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11972
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.478415138971023e-4
allele num: 6764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6916
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.685e0

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

VQSLOD
type: SiteQuality
SIO_000300: -2.623e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 4.051e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

DP
type: SiteQuality
SIO_000300: 1.189299e6

GenotypeQuality
all individuals: 505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
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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: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21577
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variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.127294043378275e-4
allele num: 44354
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.414827391058291e-4
allele num: 7068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3030
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.240131e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

MQ
type: SiteQuality
SIO_000300: 3.413e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.188e0

QD
type: SiteQuality
SIO_000300: 1.137e1

VQSLOD
type: SiteQuality
SIO_000300: -2.955e0

FS
type: SiteQuality
SIO_000300: 1.569e0

GenotypeQuality
all individuals: 863
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.108156028368794e-4
allele num: 9024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.56e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.838e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.377e0

DP
type: SiteQuality
SIO_000300: 1.374984e6

QD
type: SiteQuality
SIO_000300: 4.88e0

MQRankSum
type: SiteQuality
SIO_000300: 7.87e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 245
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13680
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.164606842199535e-5
allele num: 55830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.763e1

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.482e0

VQSLOD
type: SiteQuality
SIO_000300: -3.07e0

FS
type: SiteQuality
SIO_000300: 6.416e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

DP
type: SiteQuality
SIO_000300: 1.437224e6

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.702917217851424e-5
allele num: 57452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13930
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

FS
type: SiteQuality
SIO_000300: 7.746e0

MQ
type: SiteQuality
SIO_000300: 3.833e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.68e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

DP
type: SiteQuality
SIO_000300: 1.464557e6

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.683898561950628e-5
allele num: 59386
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.155e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.495722e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 3.607e1

QD
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.487e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.45e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 248
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GenotypeQuality
all individuals: 316
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.043623460655395e-4
allele num: 9582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.577983967682888e-5
allele num: 63372
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.591e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -2.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 3.82e1

QD
type: SiteQuality
SIO_000300: 6.77e0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11014
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.565337173627199e-5
allele num: 63884
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8514
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9676
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.579443e6

VQSLOD
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QD
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ClippingRankSum
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MQ
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SIO_000300: 3.586e1

MQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15460
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11138
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548275221403357e-5
allele num: 64588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.93e0

MQ
type: SiteQuality
SIO_000300: 3.881e1

BaseQRankSum
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SIO_000300: -1.476e0

FS
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.849e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e-1

DP
type: SiteQuality
SIO_000300: 1.593395e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.783166904422254e-4
allele num: 11216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15590
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.917e0

QD
type: SiteQuality
SIO_000300: 5.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

MQ
type: SiteQuality
SIO_000300: 4.613e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.97e-1

DP
type: SiteQuality
SIO_000300: 1.600946e6

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15912
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.68e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.837e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.26e0

MQ
type: SiteQuality
SIO_000300: 4.337e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.61612e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523368472366096e-5
allele num: 65644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-1

DP
type: SiteQuality
SIO_000300: 1.618078e6

MQ
type: SiteQuality
SIO_000300: 4.307e1

FS
type: SiteQuality
SIO_000300: 6.279e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 7.89e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65776
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
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Latino
type: Population
allele count: 1
allele frequency: 8.802816901408451e-5
allele num: 11360
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10124
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 4.422e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.623831e6

FS
type: SiteQuality
SIO_000300: 1.332e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
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SIO_000300: -2.02e0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.322340919647004e-4
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.277044854881266e-4
allele num: 11370
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.867771857114664e-5
allele num: 10134
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16040
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65808
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6358
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MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.258e1

FS
type: SiteQuality
SIO_000300: 3.294e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.305e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

DP
type: SiteQuality
SIO_000300: 1.623926e6

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 260
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GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 8

South Asian
type: Population
allele count: 21
allele frequency: 1.312664083010376e-3
allele num: 15998
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 422
allele frequency: 6.424113259247983e-3
allele num: 65690
num of homozygotes: 1

Latino
type: Population
allele count: 28
allele frequency: 2.466960352422908e-3
allele num: 11350
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.401360544217687e-3
allele num: 882
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.287383640324817e-3
allele num: 10098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.580777742649383e-3
allele num: 6326
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQ
type: SiteQuality
SIO_000300: 4.227e1

VQSLOD
type: SiteQuality
SIO_000300: -2.802e0

QD
type: SiteQuality
SIO_000300: 4.89e0

DP
type: SiteQuality
SIO_000300: 1.632543e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

FS
type: SiteQuality
SIO_000300: 1.2971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.47e-1

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

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6349
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.168567807351077e-4
allele num: 6312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.0e0

DP
type: SiteQuality
SIO_000300: 1.62343e6

QD
type: SiteQuality
SIO_000300: 1.11e1

MQ
type: SiteQuality
SIO_000300: 4.341e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

GenotypeQuality
all individuals: 45575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0