19-38709575-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709575
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709575
    reference: chr 19
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.503G>A
  hgvsp: ENSP00000397354.2:p.Cys168Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.257G>A
  hgvsp: ENSP00000391884.1:p.Cys86Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.489G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.425G>A
  hgvsp: ENSP00000411569.1:p.Cys142Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.503G>A
  hgvsp: ENSP00000347716.4:p.Cys168Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.257G>A
  hgvsp: ENSP00000399015.1:p.Cys86Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.530G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*117G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.425G>A
  hgvsp: ENSP00000390223.1:p.Cys142Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.257G>A
  hgvsp: ENSP00000416347.1:p.Cys86Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.1005G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.257G>A
  hgvsp: ENSP00000412098.1:p.Cys86Tyr
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys168Tyr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-38709583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709583
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709583
    reference: chr 19
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.495T>C
  hgvsp: ENST00000420980.2:c.495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*109T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.522T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.495T>C
  hgvsp: ENST00000355526.4:c.495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.249T>C
  hgvsp: ENST00000438365.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.249T>C
  hgvsp: ENST00000414789.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.249T>C
  hgvsp: ENST00000438060.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.249T>C
  hgvsp: ENST00000412732.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.417T>C
  hgvsp: ENST00000416611.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.417T>C
  hgvsp: ENST00000456296.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.997T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.481T>C
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile165Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-38709589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709589
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709589
    reference: chr 19
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.243G>A
  hgvsp: ENST00000414789.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.516G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.243G>A
  hgvsp: ENST00000438365.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.243G>A
  hgvsp: ENST00000438060.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.489G>A
  hgvsp: ENST00000420980.2:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.489G>A
  hgvsp: ENST00000355526.4:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.411G>A
  hgvsp: ENST00000416611.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*103G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.411G>A
  hgvsp: ENST00000456296.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.243G>A
  hgvsp: ENST00000412732.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.991G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.475G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9423
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu163Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-38709595-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709595
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709595
    reference: chr 19
allele count: 7
allele frequency: 5.767677932864229e-5
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.237G>A
  hgvsp: ENST00000412732.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.237G>A
  hgvsp: ENST00000414789.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.483G>A
  hgvsp: ENST00000355526.4:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.237G>A
  hgvsp: ENST00000438365.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.405G>A
  hgvsp: ENST00000456296.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.483G>A
  hgvsp: ENST00000420980.2:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.405G>A
  hgvsp: ENST00000416611.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.510G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.985G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.237G>A
  hgvsp: ENST00000438060.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.469G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu161Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-38709604-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709604
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709604
    reference: chr 19
allele count: 6
allele frequency: 4.943153732081068e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.976G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.228G>T
  hgvsp: ENSP00000399015.1:p.Glu76Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.501G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.396G>T
  hgvsp: ENSP00000411569.1:p.Glu132Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*88G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.474G>T
  hgvsp: ENSP00000397354.2:p.Glu158Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.396G>T
  hgvsp: ENSP00000390223.1:p.Glu132Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.228G>T
  hgvsp: ENSP00000416347.1:p.Glu76Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.460G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.474G>T
  hgvsp: ENSP00000347716.4:p.Glu158Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.228G>T
  hgvsp: ENSP00000412098.1:p.Glu76Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.228G>T
  hgvsp: ENSP00000391884.1:p.Glu76Asp
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9420
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu158Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-38709608-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709608
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709605
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.221_223delAGA
  hgvsp: ENSP00000412098.1:p.Lys74del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.389_391delAGA
  hgvsp: ENSP00000411569.1:p.Lys130del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.221_223delAGA
  hgvsp: ENSP00000416347.1:p.Lys74del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.221_223delAGA
  hgvsp: ENSP00000399015.1:p.Lys74del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.969_971delAGA
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.221_223delAGA
  hgvsp: ENSP00000391884.1:p.Lys74del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.453_455delAGA
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.467_469delAGA
  hgvsp: ENSP00000347716.4:p.Lys156del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.467_469delAGA
  hgvsp: ENSP00000397354.2:p.Lys156del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.389_391delAGA
  hgvsp: ENSP00000390223.1:p.Lys130del
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.494_496delAGA
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*81_*83delAGA
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys156del
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: ATCT
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

19-38709609-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709609
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709609
    reference: chr 19
allele count: 34
allele frequency: 2.801166603503106e-4
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.971A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.223A>G
  hgvsp: ENSP00000412098.1:p.Ile75Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.391A>G
  hgvsp: ENSP00000390223.1:p.Ile131Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*83A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.223A>G
  hgvsp: ENSP00000416347.1:p.Ile75Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.469A>G
  hgvsp: ENSP00000397354.2:p.Ile157Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.391A>G
  hgvsp: ENSP00000411569.1:p.Ile131Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.223A>G
  hgvsp: ENSP00000399015.1:p.Ile75Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.223A>G
  hgvsp: ENSP00000391884.1:p.Ile75Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.469A>G
  hgvsp: ENSP00000347716.4:p.Ile157Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.455A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.496A>G
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ile157Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-38709613-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709613
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709613
    reference: chr 19
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.219G>T
  hgvsp: ENSP00000416347.1:p.Lys73Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.492G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*79G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.465G>T
  hgvsp: ENSP00000397354.2:p.Lys155Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.967G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.219G>T
  hgvsp: ENSP00000412098.1:p.Lys73Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.387G>T
  hgvsp: ENSP00000390223.1:p.Lys129Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.387G>T
  hgvsp: ENSP00000411569.1:p.Lys129Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.465G>T
  hgvsp: ENSP00000347716.4:p.Lys155Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.451G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.219G>T
  hgvsp: ENSP00000399015.1:p.Lys73Asn
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.219G>T
  hgvsp: ENSP00000391884.1:p.Lys73Asn
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys155Asn
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

19-38709616-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709616
    reference: chr 19
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.462G>C
  hgvsp: ENSP00000347716.4:p.Glu154Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.384G>C
  hgvsp: ENSP00000390223.1:p.Glu128Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.216G>C
  hgvsp: ENSP00000412098.1:p.Glu72Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.964G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.384G>C
  hgvsp: ENSP00000411569.1:p.Glu128Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.462G>C
  hgvsp: ENSP00000397354.2:p.Glu154Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.216G>C
  hgvsp: ENSP00000391884.1:p.Glu72Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.448G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.216G>C
  hgvsp: ENSP00000416347.1:p.Glu72Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.216G>C
  hgvsp: ENSP00000399015.1:p.Glu72Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*76G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.489G>C
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9412
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu154Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/19-38709622-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709622
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709622
    reference: chr 19
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.456G>T
  hgvsp: ENST00000420980.2:c.456G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.378G>T
  hgvsp: ENST00000416611.1:c.378G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.210G>T
  hgvsp: ENST00000438365.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.483G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.456G>T
  hgvsp: ENST00000355526.4:c.456G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.210G>T
  hgvsp: ENST00000412732.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.210G>T
  hgvsp: ENST00000438060.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.442G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.210G>T
  hgvsp: ENST00000414789.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*70G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.378G>T
  hgvsp: ENST00000456296.1:c.378G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.958G>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr152Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

19-38709622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709622
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709622
    reference: chr 19
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.210G>A
  hgvsp: ENST00000438060.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.378G>A
  hgvsp: ENST00000416611.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.378G>A
  hgvsp: ENST00000456296.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.958G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.483G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.210G>A
  hgvsp: ENST00000438365.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.442G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.210G>A
  hgvsp: ENST00000414789.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.210G>A
  hgvsp: ENST00000412732.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.456G>A
  hgvsp: ENST00000355526.4:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.456G>A
  hgvsp: ENST00000420980.2:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr152Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

19-38709623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709623
    reference: chr 19
allele count: 5
allele frequency: 4.11936265221045e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.455C>T
  hgvsp: ENSP00000347716.4:p.Thr152Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.209C>T
  hgvsp: ENSP00000391884.1:p.Thr70Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.377C>T
  hgvsp: ENSP00000411569.1:p.Thr126Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.455C>T
  hgvsp: ENSP00000397354.2:p.Thr152Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.377C>T
  hgvsp: ENSP00000390223.1:p.Thr126Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.441C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.957C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.209C>T
  hgvsp: ENSP00000399015.1:p.Thr70Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.209C>T
  hgvsp: ENSP00000412098.1:p.Thr70Met
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.482C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.209C>T
  hgvsp: ENSP00000416347.1:p.Thr70Met
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr152Met
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

19-38709624-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709624
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709624
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.481A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*68A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.376A>G
  hgvsp: ENSP00000411569.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.208A>G
  hgvsp: ENSP00000391884.1:p.Thr70Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.208A>G
  hgvsp: ENSP00000399015.1:p.Thr70Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.956A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.454A>G
  hgvsp: ENSP00000397354.2:p.Thr152Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.454A>G
  hgvsp: ENSP00000347716.4:p.Thr152Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.208A>G
  hgvsp: ENSP00000412098.1:p.Thr70Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.440A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.208A>G
  hgvsp: ENSP00000416347.1:p.Thr70Ala
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.376A>G
  hgvsp: ENSP00000390223.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9410
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr152Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

19-38709628-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709628
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709628
    reference: chr 19
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.450A>C
  hgvsp: ENST00000355526.4:c.450A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.477A>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.204A>C
  hgvsp: ENST00000438365.1:c.204A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.372A>C
  hgvsp: ENST00000456296.1:c.372A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.436A>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*64A>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.450A>C
  hgvsp: ENST00000420980.2:c.450A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.952A>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.372A>C
  hgvsp: ENST00000416611.1:c.372A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.204A>C
  hgvsp: ENST00000412732.1:c.204A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.204A>C
  hgvsp: ENST00000414789.1:c.204A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.204A>C
  hgvsp: ENST00000438060.1:c.204A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala150Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

19-38709634-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709634
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709634
    reference: chr 19
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.471G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.946G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.366G>C
  hgvsp: ENST00000416611.1:c.366G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.198G>C
  hgvsp: ENST00000438365.1:c.198G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.444G>C
  hgvsp: ENST00000355526.4:c.444G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*58G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.198G>C
  hgvsp: ENST00000412732.1:c.198G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.366G>C
  hgvsp: ENST00000456296.1:c.366G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.444G>C
  hgvsp: ENST00000420980.2:c.444G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.198G>C
  hgvsp: ENST00000438060.1:c.198G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.430G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.198G>C
  hgvsp: ENST00000414789.1:c.198G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9409
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu148Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

19-38709639-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709639
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709639
    reference: chr 19
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.193C>G
  hgvsp: ENSP00000416347.1:p.Leu65Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.425C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.193C>G
  hgvsp: ENSP00000399015.1:p.Leu65Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.439C>G
  hgvsp: ENSP00000347716.4:p.Leu147Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.361C>G
  hgvsp: ENSP00000390223.1:p.Leu121Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.193C>G
  hgvsp: ENSP00000391884.1:p.Leu65Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.941C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.361C>G
  hgvsp: ENSP00000411569.1:p.Leu121Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*53C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.193C>G
  hgvsp: ENSP00000412098.1:p.Leu65Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.439C>G
  hgvsp: ENSP00000397354.2:p.Leu147Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.466C>G
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu147Val
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/19-38709640-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709640
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709640
    reference: chr 19
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.192T>G
  hgvsp: ENST00000414789.1:c.192T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.438T>G
  hgvsp: ENST00000355526.4:c.438T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.360T>G
  hgvsp: ENST00000456296.1:c.360T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.424T>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.192T>G
  hgvsp: ENST00000438060.1:c.192T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.438T>G
  hgvsp: ENST00000420980.2:c.438T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.360T>G
  hgvsp: ENST00000416611.1:c.360T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.192T>G
  hgvsp: ENST00000438365.1:c.192T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*52T>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.465T>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.192T>G
  hgvsp: ENST00000412732.1:c.192T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.940T>G
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9409
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala146Ala
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

19-38709640-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709640
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709640
    reference: chr 19
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.192T>A
  hgvsp: ENST00000438365.1:c.192T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.360T>A
  hgvsp: ENST00000456296.1:c.360T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.192T>A
  hgvsp: ENST00000438060.1:c.192T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.465T>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.438T>A
  hgvsp: ENST00000420980.2:c.438T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.192T>A
  hgvsp: ENST00000412732.1:c.192T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.192T>A
  hgvsp: ENST00000414789.1:c.192T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.438T>A
  hgvsp: ENST00000355526.4:c.438T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.360T>A
  hgvsp: ENST00000416611.1:c.360T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.424T>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*52T>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.940T>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9409
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala146Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

19-38709648-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709648
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709648
    reference: chr 19
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*44C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.430C>G
  hgvsp: ENSP00000347716.4:p.Leu144Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.352C>G
  hgvsp: ENSP00000390223.1:p.Leu118Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.430C>G
  hgvsp: ENSP00000397354.2:p.Leu144Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.184C>G
  hgvsp: ENSP00000412098.1:p.Leu62Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.932C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.416C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.184C>G
  hgvsp: ENSP00000391884.1:p.Leu62Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.457C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.184C>G
  hgvsp: ENSP00000399015.1:p.Leu62Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.352C>G
  hgvsp: ENSP00000411569.1:p.Leu118Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.184C>G
  hgvsp: ENSP00000416347.1:p.Leu62Val
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu144Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

19-38709652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709652
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709652
    reference: chr 19
allele count: 5
allele frequency: 4.12275928033114e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.180G>A
  hgvsp: ENST00000412732.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.453G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.348G>A
  hgvsp: ENST00000456296.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.928G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.180G>A
  hgvsp: ENST00000438365.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.180G>A
  hgvsp: ENST00000438060.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.180G>A
  hgvsp: ENST00000414789.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.426G>A
  hgvsp: ENST00000355526.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.426G>A
  hgvsp: ENST00000420980.2:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*40G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.348G>A
  hgvsp: ENST00000416611.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.412G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Pro142Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS

19-38709653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709653
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709653
    reference: chr 19
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.347C>T
  hgvsp: ENSP00000411569.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.452C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.411C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.179C>T
  hgvsp: ENSP00000416347.1:p.Pro60Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.425C>T
  hgvsp: ENSP00000397354.2:p.Pro142Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.179C>T
  hgvsp: ENSP00000391884.1:p.Pro60Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*39C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.425C>T
  hgvsp: ENSP00000347716.4:p.Pro142Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.179C>T
  hgvsp: ENSP00000412098.1:p.Pro60Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.927C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.179C>T
  hgvsp: ENSP00000399015.1:p.Pro60Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.347C>T
  hgvsp: ENSP00000390223.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro142Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-38709661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709661
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709661
    reference: chr 19
allele count: 2
allele frequency: 1.649783878311941e-5
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.417G>A
  hgvsp: ENST00000355526.4:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.171G>A
  hgvsp: ENST00000438365.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.919G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.171G>A
  hgvsp: ENST00000412732.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.417G>A
  hgvsp: ENST00000420980.2:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*31G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.403G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.339G>A
  hgvsp: ENST00000416611.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.171G>A
  hgvsp: ENST00000438060.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.171G>A
  hgvsp: ENST00000414789.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.339G>A
  hgvsp: ENST00000456296.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.444G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro139Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

19-38709662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709662
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709662
    reference: chr 19
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.416C>T
  hgvsp: ENSP00000347716.4:p.Pro139Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.443C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*30C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.338C>T
  hgvsp: ENSP00000411569.1:p.Pro113Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.402C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.338C>T
  hgvsp: ENSP00000390223.1:p.Pro113Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.170C>T
  hgvsp: ENSP00000412098.1:p.Pro57Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.416C>T
  hgvsp: ENSP00000397354.2:p.Pro139Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.170C>T
  hgvsp: ENSP00000416347.1:p.Pro57Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.170C>T
  hgvsp: ENSP00000399015.1:p.Pro57Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.918C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.170C>T
  hgvsp: ENSP00000391884.1:p.Pro57Leu
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro139Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

19-38709664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709664
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709664
    reference: chr 19
allele count: 2
allele frequency: 1.65016501650165e-5
allele num: 121200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.336C>T
  hgvsp: ENST00000456296.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.400C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.441C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.168C>T
  hgvsp: ENST00000414789.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.168C>T
  hgvsp: ENST00000412732.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.168C>T
  hgvsp: ENST00000438060.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.414C>T
  hgvsp: ENST00000355526.4:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.414C>T
  hgvsp: ENST00000420980.2:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.168C>T
  hgvsp: ENST00000438365.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.916C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.336C>T
  hgvsp: ENST00000416611.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*28C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu138Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-38709671-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709671
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709671
    reference: chr 19
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.161G>T
  hgvsp: ENSP00000416347.1:p.Gly54Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.393G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.161G>T
  hgvsp: ENSP00000391884.1:p.Gly54Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.329G>T
  hgvsp: ENSP00000411569.1:p.Gly110Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.161G>T
  hgvsp: ENSP00000399015.1:p.Gly54Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.161G>T
  hgvsp: ENSP00000465123.1:p.Gly54Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.407G>T
  hgvsp: ENSP00000347716.4:p.Gly136Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.434G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.329G>T
  hgvsp: ENSP00000390223.1:p.Gly110Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.909G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.161G>T
  hgvsp: ENSP00000412098.1:p.Gly54Val
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*21G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.407G>T
  hgvsp: ENSP00000397354.2:p.Gly136Val
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly136Val
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

19-38709671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709671
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709671
    reference: chr 19
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.407G>A
  hgvsp: ENSP00000347716.4:p.Gly136Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.393G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.329G>A
  hgvsp: ENSP00000390223.1:p.Gly110Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.434G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.161G>A
  hgvsp: ENSP00000412098.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.161G>A
  hgvsp: ENSP00000391884.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.161G>A
  hgvsp: ENSP00000399015.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.909G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.161G>A
  hgvsp: ENSP00000416347.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.329G>A
  hgvsp: ENSP00000411569.1:p.Gly110Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.407G>A
  hgvsp: ENSP00000397354.2:p.Gly136Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.161G>A
  hgvsp: ENSP00000465123.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly136Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/19-38709672-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709672
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709672
    reference: chr 19
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.908G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.160G>T
  hgvsp: ENSP00000412098.1:p.Gly54Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.160G>T
  hgvsp: ENSP00000399015.1:p.Gly54Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.160G>T
  hgvsp: ENSP00000465123.1:p.Gly54Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.406G>T
  hgvsp: ENSP00000347716.4:p.Gly136Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.406G>T
  hgvsp: ENSP00000397354.2:p.Gly136Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.392G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.328G>T
  hgvsp: ENSP00000411569.1:p.Gly110Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.328G>T
  hgvsp: ENSP00000390223.1:p.Gly110Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.433G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*20G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.160G>T
  hgvsp: ENSP00000416347.1:p.Gly54Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.160G>T
  hgvsp: ENSP00000391884.1:p.Gly54Cys
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly136Cys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-38709673-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709673
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709673
    reference: chr 19
allele count: 1
allele frequency: 8.263097008758882e-6
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.405G>T
  hgvsp: ENSP00000347716.4:p.Glu135Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.327G>T
  hgvsp: ENSP00000390223.1:p.Glu109Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.159G>T
  hgvsp: ENSP00000391884.1:p.Glu53Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.159G>T
  hgvsp: ENSP00000399015.1:p.Glu53Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.327G>T
  hgvsp: ENSP00000411569.1:p.Glu109Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.159G>T
  hgvsp: ENSP00000412098.1:p.Glu53Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.159G>T
  hgvsp: ENSP00000465123.1:p.Glu53Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.405G>T
  hgvsp: ENSP00000397354.2:p.Glu135Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.432G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.907G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.391G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*19G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.159G>T
  hgvsp: ENSP00000416347.1:p.Glu53Asp
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu135Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

19-38709690-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709690
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709690
    reference: chr 19
allele count: 2
allele frequency: 1.659558225600345e-5
allele num: 120514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.890G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.388G>C
  hgvsp: ENSP00000347716.4:p.Ala130Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.*2G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.142G>C
  hgvsp: ENSP00000391884.1:p.Ala48Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.415G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.310G>C
  hgvsp: ENSP00000411569.1:p.Ala104Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.142G>C
  hgvsp: ENSP00000465123.1:p.Ala48Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.388G>C
  hgvsp: ENSP00000397354.2:p.Ala130Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.142G>C
  hgvsp: ENSP00000399015.1:p.Ala48Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.142G>C
  hgvsp: ENSP00000416347.1:p.Ala48Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.310G>C
  hgvsp: ENSP00000390223.1:p.Ala104Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.142G>C
  hgvsp: ENSP00000412098.1:p.Ala48Pro
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.374G>C
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala130Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

19-38709695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709695
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709695
    reference: chr 19
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.410G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.137G>A
  hgvsp: ENSP00000416347.1:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.137G>A
  hgvsp: ENSP00000391884.1:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.305G>A
  hgvsp: ENSP00000411569.1:p.Cys102Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.383G>A
  hgvsp: ENSP00000347716.4:p.Cys128Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.383G>A
  hgvsp: ENSP00000397354.2:p.Cys128Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.137G>A
  hgvsp: ENSP00000465123.1:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.137G>A
  hgvsp: ENSP00000412098.1:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.369G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.305G>A
  hgvsp: ENSP00000390223.1:p.Cys102Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.137G>A
  hgvsp: ENSP00000399015.1:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.300G>A
  hgvsp: ENST00000418517.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.885G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys128Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP

19-38709704-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709704
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709704
    reference: chr 19
allele count: 14
allele frequency: 1.16583115433939e-4
allele num: 120086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.876C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-6C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-6C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.380-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-38709708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709708
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709708
    reference: chr 19
allele count: 1
allele frequency: 8.354916868577158e-6
allele num: 119690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.872C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-10C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-10C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

19-38709713-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709713
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709713
    reference: chr 19
allele count: 2
allele frequency: 1.672464543751672e-5
allele num: 119584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.867T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-15T>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-15T>C
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-38709714-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709714
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709715
    reference: chr 19
allele count: 13
allele frequency: 1.089982224905255e-4
allele num: 119268
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.865dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-17dupC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-17dupC
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

19-38709714-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709714
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709713
    reference: chr 19
allele count: 2
allele frequency: 1.67689573062347e-5
allele num: 119268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.865delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-17delC
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-17delC
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: TG
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-38709716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709716
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709716
    reference: chr 19
allele count: 2
allele frequency: 1.67596829067994e-5
allele num: 119334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.864C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-18C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-18C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

19-38709717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709717
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709717
    reference: chr 19
allele count: 2
allele frequency: 1.674593073883047e-5
allele num: 119432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.863C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-19C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-19C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9390
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

19-38709721-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709721
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709721
    reference: chr 19
allele count: 1
allele frequency: 8.385041086701324e-6
allele num: 119260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.859C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-23C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-23C>A
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-38709742-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709742
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709742
    reference: chr 19
allele count: 1
allele frequency: 8.472422265525714e-6
allele num: 118030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.838G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-44G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-44G>C
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-38709742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709742
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709742
    reference: chr 19
allele count: 10
allele frequency: 8.472422265525714e-5
allele num: 118030
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.838G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-44G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-44G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

19-38709743-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709743
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709743
    reference: chr 19
allele count: 2
allele frequency: 1.694226077527785e-5
allele num: 118048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.837C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-45C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-45C>G
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

19-38709743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38709743
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38709743
    reference: chr 19
allele count: 2
allele frequency: 1.694226077527785e-5
allele num: 118048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000473716
  gene symbol: DPF1
  hgvsc: ENST00000473716.1:n.837C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.134-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.380-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.380-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.302-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.366-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.297-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.134-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.134-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.407-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.134-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.134-45C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.302-45C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

19-38712947-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712947
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712947
    reference: chr 19
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+50G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+50G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

19-38712951-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712951
    reference: chr 19
allele count: 2
allele frequency: 1.652947204866277e-5
allele num: 120996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+46G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+46G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

19-38712956-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712956
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712956
    reference: chr 19
allele count: 4
allele frequency: 3.305238803503553e-5
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+41C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+41C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

19-38712958-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712958
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712958
    reference: chr 19
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+39G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+39G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

19-38712959-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712959
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712959
    reference: chr 19
allele count: 2
allele frequency: 1.652728655009421e-5
allele num: 121012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+38C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+38C>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20249
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

19-38712962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712962
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712962
    reference: chr 19
allele count: 7
allele frequency: 5.784359093012494e-5
allele num: 121016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+35C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+35C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

19-38712968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712968
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712968
    reference: chr 19
allele count: 9
allele frequency: 7.435927094865905e-5
allele num: 121034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+29G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+29G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-38712984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712984
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712984
    reference: chr 19
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+13G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+13G>A
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

19-38712986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38712986
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38712986
    reference: chr 19
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.301+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.133+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.133+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.379+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.133+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.133+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.365+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.301+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.296+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.379+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.133+11C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.406+11C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

19-38713007-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713007
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713007
    reference: chr 19
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.355G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.291G>A
  hgvsp: ENST00000416611.1:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.286G>A
  hgvsp: ENSP00000408201.1:p.Val96Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.123G>A
  hgvsp: ENST00000414789.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.396G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.123G>A
  hgvsp: ENST00000412732.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.123G>A
  hgvsp: ENST00000438060.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.291G>A
  hgvsp: ENST00000456296.1:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.369G>A
  hgvsp: ENST00000420980.2:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.123G>A
  hgvsp: ENST00000586624.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.123G>A
  hgvsp: ENST00000438365.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.369G>A
  hgvsp: ENST00000355526.4:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val96Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

19-38713015-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713015
    reference: chr 19
allele count: 4
allele frequency: 3.299839957762049e-5
allele num: 121218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.115C>A
  hgvsp: ENSP00000399015.1:p.Pro39Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.347C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.115C>A
  hgvsp: ENSP00000416347.1:p.Pro39Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.361C>A
  hgvsp: ENSP00000397354.2:p.Pro121Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.283C>A
  hgvsp: ENSP00000411569.1:p.Pro95Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.388C>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.283C>A
  hgvsp: ENSP00000390223.1:p.Pro95Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.361C>A
  hgvsp: ENSP00000347716.4:p.Pro121Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.278C>A
  hgvsp: ENSP00000408201.1:p.Ala93Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.115C>A
  hgvsp: ENSP00000465123.1:p.Pro39Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.115C>A
  hgvsp: ENSP00000391884.1:p.Pro39Thr
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.115C>A
  hgvsp: ENSP00000412098.1:p.Pro39Thr
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro121Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-38713027-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713027
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713027
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.103C>T
  hgvsp: ENSP00000465123.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.103C>T
  hgvsp: ENSP00000416347.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.103C>T
  hgvsp: ENSP00000412098.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.103C>T
  hgvsp: ENSP00000391884.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.376C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.335C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.349C>T
  hgvsp: ENSP00000347716.4:p.Pro117Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.271C>T
  hgvsp: ENSP00000390223.1:p.Pro91Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.271C>T
  hgvsp: ENSP00000411569.1:p.Pro91Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.349C>T
  hgvsp: ENSP00000397354.2:p.Pro117Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.266C>T
  hgvsp: ENSP00000408201.1:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.103C>T
  hgvsp: ENSP00000399015.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro117Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-38713034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713034
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713034
    reference: chr 19
allele count: 6
allele frequency: 4.950658437572197e-5
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.369G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.342G>A
  hgvsp: ENST00000355526.4:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.328G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.96G>A
  hgvsp: ENST00000438060.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.264G>A
  hgvsp: ENST00000456296.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.96G>A
  hgvsp: ENST00000412732.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.96G>A
  hgvsp: ENST00000438365.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.264G>A
  hgvsp: ENST00000416611.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.96G>A
  hgvsp: ENST00000414789.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.259G>A
  hgvsp: ENSP00000408201.1:p.Gly87Arg
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.96G>A
  hgvsp: ENST00000586624.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.342G>A
  hgvsp: ENST00000420980.2:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20271
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly87Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-38713041-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713041
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713041
    reference: chr 19
allele count: 22
allele frequency: 1.81575081296116e-4
allele num: 121162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.89A>G
  hgvsp: ENSP00000416347.1:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.321A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.89A>G
  hgvsp: ENSP00000412098.1:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.89A>G
  hgvsp: ENSP00000465123.1:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.89A>G
  hgvsp: ENSP00000399015.1:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.362A>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.257A>G
  hgvsp: ENSP00000411569.1:p.Asn86Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.335A>G
  hgvsp: ENSP00000347716.4:p.Asn112Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.335A>G
  hgvsp: ENSP00000397354.2:p.Asn112Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.257A>G
  hgvsp: ENSP00000390223.1:p.Asn86Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.89A>G
  hgvsp: ENSP00000391884.1:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.252A>G
  hgvsp: ENST00000418517.1:c.252A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn112Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-38713047-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713047
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713047
    reference: chr 19
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.83G>T
  hgvsp: ENSP00000465123.1:p.Arg28Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.83G>T
  hgvsp: ENSP00000391884.1:p.Arg28Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.329G>T
  hgvsp: ENSP00000397354.2:p.Arg110Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.83G>T
  hgvsp: ENSP00000399015.1:p.Arg28Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.315G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.246G>T
  hgvsp: ENSP00000408201.1:p.Glu82Asp
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.329G>T
  hgvsp: ENSP00000347716.4:p.Arg110Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.251G>T
  hgvsp: ENSP00000411569.1:p.Arg84Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.83G>T
  hgvsp: ENSP00000416347.1:p.Arg28Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.356G>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.251G>T
  hgvsp: ENSP00000390223.1:p.Arg84Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.83G>T
  hgvsp: ENSP00000412098.1:p.Arg28Ile
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg110Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-38713050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713050
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713050
    reference: chr 19
allele count: 2
allele frequency: 1.65174589541145e-5
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.326G>A
  hgvsp: ENSP00000347716.4:p.Arg109Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.243G>A
  hgvsp: ENST00000418517.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.80G>A
  hgvsp: ENSP00000399015.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.248G>A
  hgvsp: ENSP00000411569.1:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.80G>A
  hgvsp: ENSP00000412098.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.353G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.248G>A
  hgvsp: ENSP00000390223.1:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.312G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.326G>A
  hgvsp: ENSP00000397354.2:p.Arg109Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.80G>A
  hgvsp: ENSP00000465123.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.80G>A
  hgvsp: ENSP00000416347.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.80G>A
  hgvsp: ENSP00000391884.1:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg109Gln
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

19-38713058-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713058
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713058
    reference: chr 19
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.72G>A
  hgvsp: ENST00000586624.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.235G>A
  hgvsp: ENSP00000408201.1:p.Glu79Lys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.72G>A
  hgvsp: ENST00000412732.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.240G>A
  hgvsp: ENST00000416611.1:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.318G>A
  hgvsp: ENST00000355526.4:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.72G>A
  hgvsp: ENST00000438060.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.240G>A
  hgvsp: ENST00000456296.1:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.304G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.345G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.318G>A
  hgvsp: ENST00000420980.2:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.72G>A
  hgvsp: ENST00000438365.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.72G>A
  hgvsp: ENST00000414789.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu79Lys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS

19-38713073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713073
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713073
    reference: chr 19
allele count: 2
allele frequency: 1.657934876318058e-5
allele num: 120632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.225C>T
  hgvsp: ENST00000416611.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.289C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.57C>T
  hgvsp: ENST00000586624.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.303C>T
  hgvsp: ENST00000355526.4:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.225C>T
  hgvsp: ENST00000456296.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.57C>T
  hgvsp: ENST00000438060.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.220C>T
  hgvsp: ENSP00000408201.1:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.57C>T
  hgvsp: ENST00000438365.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.57C>T
  hgvsp: ENST00000414789.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.57C>T
  hgvsp: ENST00000412732.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.330C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.303C>T
  hgvsp: ENST00000420980.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg74Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

19-38713079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713079
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713079
    reference: chr 19
allele count: 1
allele frequency: 8.30357884248111e-6
allele num: 120430
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.51G>A
  hgvsp: ENST00000586624.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.219G>A
  hgvsp: ENST00000416611.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.51G>A
  hgvsp: ENST00000438365.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.219G>A
  hgvsp: ENST00000456296.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.51G>A
  hgvsp: ENST00000438060.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.297G>A
  hgvsp: ENST00000420980.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.51G>A
  hgvsp: ENST00000414789.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.283G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.214G>A
  hgvsp: ENSP00000408201.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.51G>A
  hgvsp: ENST00000412732.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.324G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.297G>A
  hgvsp: ENST00000355526.4:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 19986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8319
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val72Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ

19-38713082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713082
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713082
    reference: chr 19
allele count: 1
allele frequency: 8.311999202048076e-6
allele num: 120308
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.294C>T
  hgvsp: ENST00000355526.4:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.216C>T
  hgvsp: ENST00000456296.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.48C>T
  hgvsp: ENST00000438060.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.321C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.294C>T
  hgvsp: ENST00000420980.2:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.48C>T
  hgvsp: ENST00000412732.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.216C>T
  hgvsp: ENST00000416611.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.48C>T
  hgvsp: ENST00000586624.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.48C>T
  hgvsp: ENST00000438365.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.48C>T
  hgvsp: ENST00000414789.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.280C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.211C>T
  hgvsp: ENSP00000408201.1:p.His71Tyr
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21354
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His71Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-38713094-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713094
    reference: chr 19
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.268G>C
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.36G>C
  hgvsp: ENST00000438365.1:c.36G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.199G>C
  hgvsp: ENSP00000408201.1:p.Gly67Arg
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.36G>C
  hgvsp: ENST00000414789.1:c.36G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.36G>C
  hgvsp: ENST00000586624.1:c.36G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.282G>C
  hgvsp: ENST00000355526.4:c.282G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.204G>C
  hgvsp: ENST00000416611.1:c.204G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.36G>C
  hgvsp: ENST00000438060.1:c.36G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.204G>C
  hgvsp: ENST00000456296.1:c.204G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.36G>C
  hgvsp: ENST00000412732.1:c.36G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.282G>C
  hgvsp: ENST00000420980.2:c.282G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.309G>C
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly67Arg
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD

19-38713094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713094
    reference: chr 19
allele count: 3
allele frequency: 2.508151492350138e-5
allele num: 119610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.204G>A
  hgvsp: ENST00000416611.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.199G>A
  hgvsp: ENSP00000408201.1:p.Gly67Arg
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.36G>A
  hgvsp: ENST00000586624.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.204G>A
  hgvsp: ENST00000456296.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.268G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.36G>A
  hgvsp: ENST00000412732.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.36G>A
  hgvsp: ENST00000438060.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.282G>A
  hgvsp: ENST00000355526.4:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.36G>A
  hgvsp: ENST00000438365.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.309G>A
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.282G>A
  hgvsp: ENST00000420980.2:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.36G>A
  hgvsp: ENST00000414789.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly67Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

19-38713097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713097
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713097
    reference: chr 19
allele count: 1
allele frequency: 8.380262805041566e-6
allele num: 119328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.33C>T
  hgvsp: ENST00000438060.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.33C>T
  hgvsp: ENST00000438365.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.279C>T
  hgvsp: ENST00000420980.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.279C>T
  hgvsp: ENST00000355526.4:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.33C>T
  hgvsp: ENST00000414789.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.201C>T
  hgvsp: ENST00000416611.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.265C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.201C>T
  hgvsp: ENST00000456296.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.196C>T
  hgvsp: ENSP00000408201.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.33C>T
  hgvsp: ENST00000586624.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.33C>T
  hgvsp: ENST00000412732.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.306C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro66Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-38713107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713107
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713107
    reference: chr 19
allele count: 1
allele frequency: 8.452513777597457e-6
allele num: 118308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.26-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.258-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.299-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.26-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.26-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.272-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.189-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.26-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.194-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.194-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.26-3C>T
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.272-3C>T
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.272-3C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

19-38713108-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38713108
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 38713108
    reference: chr 19
allele count: 1
allele frequency: 8.45394291897741e-6
allele num: 118288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000391884
  ensembl transcript: ENST00000414789
  gene symbol: DPF1
  hgvsc: ENST00000414789.1:c.26-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000416347
  ensembl transcript: ENST00000438060
  gene symbol: DPF1
  hgvsc: ENST00000438060.1:c.26-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000390223
  ensembl transcript: ENST00000416611
  gene symbol: DPF1
  hgvsc: ENST00000416611.1:c.194-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000347716
  ensembl transcript: ENST00000355526
  gene symbol: DPF1
  hgvsc: ENST00000355526.4:c.272-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000412098
  ensembl transcript: ENST00000412732
  gene symbol: DPF1
  hgvsc: ENST00000412732.1:c.26-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000475938
  gene symbol: DPF1
  hgvsc: ENST00000475938.1:n.258-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000408201
  ensembl transcript: ENST00000418517
  gene symbol: DPF1
  hgvsc: ENST00000418517.1:c.189-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000411569
  ensembl transcript: ENST00000456296
  gene symbol: DPF1
  hgvsc: ENST00000456296.1:c.194-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000397354
  ensembl transcript: ENST00000420980
  gene symbol: DPF1
  hgvsc: ENST00000420980.2:c.272-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl transcript: ENST00000471976
  gene symbol: DPF1
  hgvsc: ENST00000471976.1:n.299-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000399015
  ensembl transcript: ENST00000438365
  gene symbol: DPF1
  hgvsc: ENST00000438365.1:c.26-4C>G
  variant of: http://identifiers.org/hgnc/20225
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000011332
  ensembl protein: ENSP00000465123
  ensembl transcript: ENST00000586624
  gene symbol: DPF1
  hgvsc: ENST00000586624.1:c.26-4C>G
  variant of: http://identifiers.org/hgnc/20225
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
hgvs: c.272-4C>G
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 9423
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2501
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1942
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47490
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 737
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.612e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

DP
type: SiteQuality
SIO_000300: 4.126108e6

QD
type: SiteQuality
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MQ
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SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
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SIO_000300: 5.02e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: 3.75e0

ClippingRankSum
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VQSLOD
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QD
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FS
type: SiteQuality
SIO_000300: 6.99e-1

ReadPosRankSum
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SIO_000300: -1.55e-1

DP
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SIO_000300: 4.127197e6

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

African
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allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
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SIO_000300: 1.03e0

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.952e1

FS
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SIO_000300: 1.273e0

DP
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SIO_000300: 4.12744e6

ReadPosRankSum
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SIO_000300: -7.96e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 8.995232526760817e-5
allele num: 66702
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

East Asian
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ClippingRankSum
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SIO_000300: -2.5e-2

ReadPosRankSum
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VQSLOD
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QD
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FS
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MQ
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BaseQRankSum
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MQRankSum
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DP
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SIO_000300: 4.127714e6

InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

East Asian
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allele count: 0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 6
allele frequency: 8.993344924755681e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66716
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

South Asian
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FS
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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variant carriers: 3

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
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European (Finnish)
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num of homozygotes: 0

Other
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South Asian
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allele num: 16510
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

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

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

Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66714
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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East Asian
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African
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VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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SIO_000300: 1.37e0

FS
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SIO_000300: 1.04e0

MQ
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SIO_000300: 5.978e1

ClippingRankSum
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SIO_000300: -8.78e-1

DP
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SIO_000300: 4.127254e6

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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BaseQRankSum
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SIO_000300: 9.27e-1

MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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QD
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GenotypeDepth
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variant carriers: 1

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

African
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East Asian
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Other
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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VQSLOD
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QD
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BaseQRankSum
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MQ
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SIO_000300: 5.946e1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

African
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Other
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Latino
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European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

European (Finnish)
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East Asian
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 5.542e0

DP
type: SiteQuality
SIO_000300: 4.126742e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.24e-1

GenotypeDepth
all individuals: 1539
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3482
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variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47465
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 416
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 1.178e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

DP
type: SiteQuality
SIO_000300: 4.12633e6

GenotypeDepth
all individuals: 4767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2580
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variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
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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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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: 4.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 877
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

DP
type: SiteQuality
SIO_000300: 4.126723e6

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

FS
type: SiteQuality
SIO_000300: 1.771e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.017e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeDepth
all individuals: 3364
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 47464
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.885170225043277e-4
allele num: 10398
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

DP
type: SiteQuality
SIO_000300: 4.126723e6

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

QD
type: SiteQuality
SIO_000300: 1.017e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

FS
type: SiteQuality
SIO_000300: 1.771e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeDepth
all individuals: 3025
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4767
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variant carriers: 0

GenotypeDepth
all individuals: 3364
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.118e1

BaseQRankSum
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SIO_000300: -4.033e0

DP
type: SiteQuality
SIO_000300: 4.125268e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

FS
type: SiteQuality
SIO_000300: 3.5e0

VQSLOD
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

GenotypeDepth
all individuals: 3024
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3364
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 8.25e1
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GenotypeQuality
all individuals: 47465
bin: 9.75e1
variant carriers: 5

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.999160117583539e-5
allele num: 66676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.098e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
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SIO_000300: 2.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

DP
type: SiteQuality
SIO_000300: 4.123954e6

FS
type: SiteQuality
SIO_000300: 2.47e0

GenotypeDepth
all individuals: 4767
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2110
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.123483e6

MQRankSum
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SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 1.396e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e0

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 413
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.072109407376709e-4
allele num: 9652
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65774
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.064834e6

ClippingRankSum
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VQSLOD
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SIO_000300: 6.22e-1

BaseQRankSum
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SIO_000300: 2.97e0

MQRankSum
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SIO_000300: 7.28e-1

FS
type: SiteQuality
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MQ
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SIO_000300: 5.914e1

ReadPosRankSum
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SIO_000300: 1.0e0

QD
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SIO_000300: 1.38e1

InbreedingCoeff
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SIO_000300: 8.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65812
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.738e1

FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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SIO_000300: 7.48e-1

MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521005080156968e-5
allele num: 65746
num of homozygotes: 0

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

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

QD
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SIO_000300: 1.364e1

InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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DP
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SIO_000300: 4.055634e6

FS
type: SiteQuality
SIO_000300: 4.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

MQRankSum
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SIO_000300: 3.0e-3

ClippingRankSum
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SIO_000300: -1.133e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.221226825930074e-5
allele num: 16074
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65100
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.394e1

VQSLOD
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DP
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SIO_000300: 4.020479e6

MQ
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InbreedingCoeff
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FS
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SIO_000300: 9.95e-1

ClippingRankSum
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MQRankSum
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SIO_000300: -5.9e-2

BaseQRankSum
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SIO_000300: 6.66e-1

ReadPosRankSum
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SIO_000300: -4.47e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65100
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

East Asian
type: Population
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allele frequency: 1.166316771635176e-3
allele num: 8574
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65106
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 1.737921445950643e-4
allele num: 11508
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
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African
type: Population
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allele frequency: 1.076658053402239e-4
allele num: 9288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535956747457992e-5
allele num: 65106
num of homozygotes: 0

East Asian
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Other
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allele frequency: 0.0e0
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Latino
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

DP
type: SiteQuality
SIO_000300: 4.01966e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.11e0

ClippingRankSum
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SIO_000300: -1.664e0

VQSLOD
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.363e1

DP
type: SiteQuality
SIO_000300: 1.866447e6

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66534
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.324500232450023e-4
allele num: 8604
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

DP
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SIO_000300: 1.866392e6

MQRankSum
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SIO_000300: -6.58e-1

QD
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ReadPosRankSum
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 4.304e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.1e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.866809e6

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
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SIO_000300: -6.58e-1

ReadPosRankSum
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SIO_000300: 1.43e0

BaseQRankSum
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SIO_000300: -3.38e0

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

FS
type: SiteQuality
SIO_000300: 2.024e0

QD
type: SiteQuality
SIO_000300: 1.567e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.988e1

DP
type: SiteQuality
SIO_000300: 1.86644e6

MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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SIO_000300: -1.23e-2

ReadPosRankSum
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SIO_000300: 1.52e0

FS
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SIO_000300: 7.871e0

ClippingRankSum
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SIO_000300: -1.557e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.32396002788752e-4
allele num: 8606
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.283e1

ClippingRankSum
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SIO_000300: 1.52e-1

InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
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SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 1.866766e6

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 6
allele frequency: 3.646086533787069e-4
allele num: 16456
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 9
allele frequency: 7.790858725761773e-4
allele num: 11552
num of homozygotes: 1

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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East Asian
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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DP
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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QD
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DP
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.500690317546071e-5
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Latino
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African
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East Asian
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South Asian
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Other
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InbreedingCoeff
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DP
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 908
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Latino
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allele frequency: 3.459609064175748e-4
allele num: 11562
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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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QD
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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MQ
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ClippingRankSum
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DP
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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African
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Other
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FS
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ClippingRankSum
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MQ
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DP
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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South Asian
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East Asian
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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FS
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Other
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Latino
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South Asian
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European (Non-Finnish)
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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East Asian
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South Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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VQSLOD
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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Latino
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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European (Non-Finnish)
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European (Finnish)
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African
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allele num: 10348
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Latino
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ReadPosRankSum
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SIO_000300: 1.78e-1

BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Latino
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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African
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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South Asian
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Latino
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African
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European (Finnish)
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QD
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

DP
type: SiteQuality
SIO_000300: 1.820997e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

FS
type: SiteQuality
SIO_000300: 1.028e0

QD
type: SiteQuality
SIO_000300: 1.302e1

GenotypeDepth
all individuals: 67
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 777
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 36315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12897
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.333722287047841e-4
allele num: 8570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516898246465627e-5
allele num: 65924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15868
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.820997e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 7.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

FS
type: SiteQuality
SIO_000300: 1.028e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.302e1

VQSLOD
type: SiteQuality
SIO_000300: 9.51e-1

GenotypeDepth
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 481
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520912547528517e-5
allele num: 65750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.031e0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 4.789e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.96e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

DP
type: SiteQuality
SIO_000300: 1.811334e6

GenotypeDepth
all individuals: 65
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12592
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35039
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65202
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.384065372829418e-5
allele num: 15664
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

VQSLOD
type: SiteQuality
SIO_000300: -2.602e0

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

FS
type: SiteQuality
SIO_000300: 1.506e0

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

DP
type: SiteQuality
SIO_000300: 1.791586e6

MQ
type: SiteQuality
SIO_000300: 5.836e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1