16-72143344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143344
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143344
    reference: chr 16
allele count: 1
allele frequency: 8.35952651641811e-6
allele num: 119624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.303G>A
  hgvsp: ENSP00000454521.2:p.Gly102Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.379G>A
  hgvsp: ENSP00000462397.1:p.Gly127Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*927G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3276G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.327G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.603G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3412G>A
  hgvsp: ENSP00000268482.3:p.Gly1138Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1348G>A
  hgvsp: ENSP00000437898.1:p.Gly450Arg
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3106
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly1138Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

16-72143357-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143357
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143357
    reference: chr 16
allele count: 4729
allele frequency: 7.921007671434793e-2
allele num: 59702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.316C>G
  hgvsp: ENSP00000454521.2:p.Ala106Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.616C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.392C>G
  hgvsp: ENSP00000462397.1:p.Ala131Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3425C>G
  hgvsp: ENSP00000268482.3:p.Ala1142Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1361C>G
  hgvsp: ENSP00000437898.1:p.Ala454Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3263C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*940C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.340C>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 12278
  bin: 2.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 6544
  bin: 3.75e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 11547
  bin: 2.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.25e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 365
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 4.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 362
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 5.25e1
  variant carriers: 452
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 1.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 9.75e1
  variant carriers: 773
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 123
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 2.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 1.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 2.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 3.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 1.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 5.75e1
  variant carriers: 16
hgvs: p.Ala1142Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-72143357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143357
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143357
    reference: chr 16
allele count: 3
allele frequency: 5.024957287863053e-5
allele num: 59702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1361C>T
  hgvsp: ENSP00000437898.1:p.Ala454Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3263C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.316C>T
  hgvsp: ENSP00000454521.2:p.Ala106Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.392C>T
  hgvsp: ENSP00000462397.1:p.Ala131Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.616C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*940C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3425C>T
  hgvsp: ENSP00000268482.3:p.Ala1142Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.340C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 6544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5021
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ala1142Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

16-72143358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143358
    reference: chr 16
allele count: 6
allele frequency: 5.039475894506971e-5
allele num: 119060
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3426G>A
  hgvsp: ENST00000268482.3:c.3426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.341G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*941G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.317G>A
  hgvsp: ENST00000567142.2:c.317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.617G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3262G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1362G>A
  hgvsp: ENST00000536867.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.393G>A
  hgvsp: ENST00000563819.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2759
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5609
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala1142Ala
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-72143359-GAGCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143359
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143355
    reference: chr 16
allele count: 710
allele frequency: 5.962177958415908e-3
allele num: 119084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*943_*946delAGCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3428_3431delAGCT
  hgvsp: ENSP00000268482.3:p.Glu1143GlyfsTer8
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.395_398delAGCT
  hgvsp: ENSP00000462397.1:p.Glu132GlyfsTer8
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1364_1367delAGCT
  hgvsp: ENSP00000437898.1:p.Glu455GlyfsTer8
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3260_313-3257delAGCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.319_322delAGCT
  hgvsp: ENSP00000454521.2:p.Glu107GlyfsTer8
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.343_346delAGCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.619_622delAGCT
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 16938
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19682
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 31814
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 2
hgvs: p.Glu1143GlyfsTer8
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: GAGCT
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-72143360-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143360
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143360
    reference: chr 16
allele count: 3825
allele frequency: 3.398248014357043e-2
allele num: 112558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.395A>G
  hgvsp: ENSP00000462397.1:p.Glu132Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.619A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.343A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3428A>G
  hgvsp: ENSP00000268482.3:p.Glu1143Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.319A>G
  hgvsp: ENSP00000454521.2:p.Glu107Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1364A>G
  hgvsp: ENSP00000437898.1:p.Glu455Gly
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*943A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3260A>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 3.75e1
  variant carriers: 471
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.5e0
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 1.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 17918
  bin: 2.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 3.25e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 20631
  bin: 2.75e1
  variant carriers: 258
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 1.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 305
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 350
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 390
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 77
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 1.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 30737
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 7.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 2.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 11
hgvs: p.Glu1143Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-72143361-GCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143359
    reference: chr 16
allele count: 259
allele frequency: 2.212427177831309e-3
allele num: 117066
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1366_1367delCT
  hgvsp: ENSP00000437898.1:p.Leu456GlyfsTer6
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*945_*946delCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.345_346delCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.621_622delCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3430_3431delCT
  hgvsp: ENSP00000268482.3:p.Leu1144GlyfsTer6
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.397_398delCT
  hgvsp: ENSP00000462397.1:p.Leu133GlyfsTer6
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3258_313-3257delCT
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.321_322delCT
  hgvsp: ENSP00000454521.2:p.Leu108GlyfsTer6
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 7598
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 21997
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 18756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu1144GlyfsTer6
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: GCT
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

16-72143362-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143362
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143362
    reference: chr 16
allele count: 45
allele frequency: 3.891185168531553e-4
allele num: 115646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.345C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.621C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.321C>G
  hgvsp: ENSP00000454521.2:p.Leu108Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1366C>G
  hgvsp: ENSP00000437898.1:p.Leu456Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3258C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.397C>G
  hgvsp: ENSP00000462397.1:p.Leu133Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3430C>G
  hgvsp: ENSP00000268482.3:p.Leu1144Val
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*945C>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7708
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu1144Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-72143363-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143363
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143363
    reference: chr 16
allele count: 43
allele frequency: 3.713106402086248e-4
allele num: 115806
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.622T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.322T>G
  hgvsp: ENSP00000454521.2:p.Leu108Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1367T>G
  hgvsp: ENSP00000437898.1:p.Leu456Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.346T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3257T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.398T>G
  hgvsp: ENSP00000462397.1:p.Leu133Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3431T>G
  hgvsp: ENSP00000268482.3:p.Leu1144Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*946T>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 18859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7686
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu1144Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-72143368-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143368
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143368
    reference: chr 16
allele count: 1
allele frequency: 8.454228805248384e-6
allele num: 118284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*951C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3252C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.327C>A
  hgvsp: ENSP00000454521.2:p.Pro110Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1372C>A
  hgvsp: ENSP00000437898.1:p.Pro458Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.351C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3436C>A
  hgvsp: ENSP00000268482.3:p.Pro1146Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.627C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.403C>A
  hgvsp: ENSP00000462397.1:p.Pro135Thr
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2773
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36168
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro1146Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-72143382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143382
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143382
    reference: chr 16
allele count: 48
allele frequency: 4.096192247956171e-4
allele num: 117182
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3450C>T
  hgvsp: ENST00000268482.3:c.3450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*965C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.365C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1386C>T
  hgvsp: ENST00000536867.1:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.641C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.341C>T
  hgvsp: ENST00000567142.2:c.341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.417C>T
  hgvsp: ENST00000563819.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3238C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21988
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7366
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19295
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2770
  bin: 9.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser1150Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-72143394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143394
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143394
    reference: chr 16
allele count: 3
allele frequency: 2.599563273370074e-5
allele num: 115404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1398G>A
  hgvsp: ENST00000536867.1:c.1398G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*977G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3462G>A
  hgvsp: ENST00000268482.3:c.3462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.653G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3226G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.353G>A
  hgvsp: ENST00000567142.2:c.353G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.377G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.429G>A
  hgvsp: ENST00000563819.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17429
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala1154Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-72143399-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143399
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143399
    reference: chr 16
allele count: 1
allele frequency: 8.759328685049578e-6
allele num: 114164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.358A>C
  hgvsp: ENSP00000454521.2:p.Lys120Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3467A>C
  hgvsp: ENSP00000268482.3:p.Lys1156Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3221A>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.434A>C
  hgvsp: ENSP00000462397.1:p.Lys145Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.382A>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*982A>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1403A>C
  hgvsp: ENSP00000437898.1:p.Lys468Thr
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.658A>C
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6310
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys1156Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/16-72143402-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143402
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143402
    reference: chr 16
allele count: 1
allele frequency: 8.830645873439184e-6
allele num: 113242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.385C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.437C>A
  hgvsp: ENSP00000462397.1:p.Ser146Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1406C>A
  hgvsp: ENSP00000437898.1:p.Ser469Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3470C>A
  hgvsp: ENSP00000268482.3:p.Ser1157Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*985C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.361C>A
  hgvsp: ENSP00000454521.2:p.Ser121Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3218C>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.661C>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5898
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7830
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser1157Ter
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

16-72143406-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143406
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143406
    reference: chr 16
allele count: 650
allele frequency: 5.783947321587471e-3
allele num: 112380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.389G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1410G>C
  hgvsp: ENST00000536867.1:c.1410G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.441G>C
  hgvsp: ENST00000563819.1:c.441G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3214G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*989G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.665G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.365G>C
  hgvsp: ENST00000567142.2:c.365G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3474G>C
  hgvsp: ENST00000268482.3:c.3474G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 1.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 3.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 17788
  bin: 2.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 1.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.25e1
  variant carriers: 102
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1158Arg
num of homozygotes: 1
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-72143406-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143406
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143406
    reference: chr 16
allele count: 1
allele frequency: 8.898380494749955e-6
allele num: 112380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.665G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.365G>T
  hgvsp: ENST00000567142.2:c.365G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.389G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*989G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.441G>T
  hgvsp: ENST00000563819.1:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1410G>T
  hgvsp: ENST00000536867.1:c.1410G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3474G>T
  hgvsp: ENST00000268482.3:c.3474G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3214G>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1158Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

16-72143407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143407
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143407
    reference: chr 16
allele count: 1
allele frequency: 8.918697156719347e-6
allele num: 112124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.666C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.366C>T
  hgvsp: ENSP00000454521.2:p.Gln123Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*990C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.442C>T
  hgvsp: ENSP00000462397.1:p.Gln148Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.390C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3475C>T
  hgvsp: ENSP00000268482.3:p.Gln1159Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1411C>T
  hgvsp: ENSP00000437898.1:p.Gln471Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3213C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16085
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8972
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln1159Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

16-72143411-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143411
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143411
    reference: chr 16
allele count: 665
allele frequency: 6.389807056653087e-3
allele num: 104072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+2T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.394T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+2T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+2T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+2T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+2T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3209T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+2T>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.75e1
  variant carriers: 230
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15410
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 16591
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 9571
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 7.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 6.75e1
  variant carriers: 4
hgvs: c.3477+2T>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-72143413-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143413
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143413
    reference: chr 16
allele count: 530
allele frequency: 4.848507025761124e-3
allele num: 109312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.396A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+4A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+4A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+4A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+4A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3207A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+4A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+4A>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 16536
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16275
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4776
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10851
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 28508
  bin: 6.25e1
  variant carriers: 0
hgvs: c.3477+4A>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

16-72143414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143414
    reference: chr 16
allele count: 1461
allele frequency: 1.331668368091002e-2
allele num: 109712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+5G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.397G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+5G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+5G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+5G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+5G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3206G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+5G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 16348
  bin: 2.75e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 15977
  bin: 2.25e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 10282
  bin: 1.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 1.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 3.25e1
  variant carriers: 183
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 7.75e1
  variant carriers: 7
hgvs: c.3477+5G>A
num of homozygotes: 16
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-72143419-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143419
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143419
    reference: chr 16
allele count: 1
allele frequency: 9.285740816402333e-6
allele num: 107692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+10C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.402C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+10C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+10C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3201C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+10C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+10C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+10C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-72143421-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143421
    reference: chr 16
allele count: 1
allele frequency: 9.31098696461825e-6
allele num: 107400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+12G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+12G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+12G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+12G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.404G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3199G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+12G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+12G>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12923
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14559
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-72143422-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143422
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143422
    reference: chr 16
allele count: 3
allele frequency: 2.798455252700509e-5
allele num: 107202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+13T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3198T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+13T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+13T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+13T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.405T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+13T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+13T>C
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15013
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

16-72143425-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143425
    reference: chr 16
allele count: 1
allele frequency: 9.386498460614252e-6
allele num: 106536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+16T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+16T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+16T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+16T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.408T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+16T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+16T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3195T>C
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15964
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3826
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

16-72143425-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143425
    reference: chr 16
allele count: 1
allele frequency: 9.386498460614252e-6
allele num: 106536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3195T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+16T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.408T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+16T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+16T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+16T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+16T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+16T>G
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12932
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15964
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

16-72143426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143426
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143426
    reference: chr 16
allele count: 6
allele frequency: 5.648441030275644e-5
allele num: 106224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+17C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+17C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+17C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+17C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+17C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.409C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+17C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3194C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16083
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11613
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3945
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4042
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum

16-72143428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143428
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143428
    reference: chr 16
allele count: 1
allele frequency: 9.449652252797097e-6
allele num: 105824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+19T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3192T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+19T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.411T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+19T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+19T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+19T>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+19T>C
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11208
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-72143429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143429
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143429
    reference: chr 16
allele count: 1
allele frequency: 9.510042604990871e-6
allele num: 105152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+20C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+20C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+20C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3191C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.412C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+20C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+20C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+20C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-72143430-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143430
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143430
    reference: chr 16
allele count: 1
allele frequency: 9.543623904869157e-6
allele num: 104782
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+21G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+21G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+21G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.413G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+21G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+21G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3190G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+21G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-72143431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143431
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143431
    reference: chr 16
allele count: 8
allele frequency: 7.626892422682378e-5
allele num: 104892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+22C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+22C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+22C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.414C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+22C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+22C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3189C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+22C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10555
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10790
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18012
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4746
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

16-72143436-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143436
    reference: chr 16
allele count: 2
allele frequency: 1.928305597871151e-5
allele num: 103718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+27G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+27G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3184G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+27G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+27G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+27G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+27G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.419G>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18870
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5696
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5182
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

16-72143441-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143441
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143441
    reference: chr 16
allele count: 39
allele frequency: 3.822330249333543e-4
allele num: 102032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+32G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3179G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+32G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+32G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.424G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+32G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+32G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+32G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8082
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21184
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6571
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19493
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

16-72143451-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143451
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143451
    reference: chr 16
allele count: 1
allele frequency: 1.02519940128355e-5
allele num: 97542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3169G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+42G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+42G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.434G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+42G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+42G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+42G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+42G>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-72143453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143453
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143453
    reference: chr 16
allele count: 1
allele frequency: 1.03538961711292e-5
allele num: 96582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+44G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+44G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3167G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.436G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+44G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+44G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+44G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+44G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10294
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

16-72143454-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143454
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143454
    reference: chr 16
allele count: 2
allele frequency: 2.080213013812614e-5
allele num: 96144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+45G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.437G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+45G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+45G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+45G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3166G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+45G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+45G>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20302
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-72143456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143456
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143456
    reference: chr 16
allele count: 9
allele frequency: 9.474282586268607e-5
allele num: 94994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+47C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+47C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3164C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+47C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+47C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.439C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+47C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+47C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20137
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5419
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17631
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

16-72143457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143457
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143457
    reference: chr 16
allele count: 16
allele frequency: 1.697396617937239e-4
allele num: 94262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.440G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3163G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+48G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+48G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+48G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+48G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+48G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+48G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20056
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13073
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 9.75e1
  variant carriers: 13
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

16-72143461-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72143461
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72143461
    reference: chr 16
allele count: 1
allele frequency: 1.117443289753045e-5
allele num: 89490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-3159T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.668+52T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1413+52T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*992+52T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3477+52T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000569952
  gene symbol: DHX38
  hgvsc: ENST00000569952.1:n.444T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.444+52T>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.368+52T>G
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19681
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5769
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12448
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

16-72144815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144815
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144815
    reference: chr 16
allele count: 1
allele frequency: 3.769601930036188e-5
allele num: 26528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993-40G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369-40G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-127G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414-40G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478-40G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1805G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669-40G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14612
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5681
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

16-72144825-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144825
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144825
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 27324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1795G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369-30G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478-30G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669-30G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993-30G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414-30G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-117G>C
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29248
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17060
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4679
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13953
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

16-72144831-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144831
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144831
    reference: chr 16
allele count: 1
allele frequency: 3.576282097131822e-5
allele num: 27962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-111G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1789G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478-24G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993-24G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369-24G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414-24G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669-24G>C
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13002
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-72144849-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144849
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144849
    reference: chr 16
allele count: 3
allele frequency: 9.651888552860177e-5
allele num: 31082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669-6C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-93C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369-6C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993-6C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414-6C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1771C>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478-6C>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34159
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
hgvs: c.3478-6C>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD

16-72144849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144849
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144849
    reference: chr 16
allele count: 2
allele frequency: 6.43459236857345e-5
allele num: 31082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1771C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414-6C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369-6C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-93C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993-6C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669-6C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478-6C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8017
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
hgvs: c.3478-6C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

16-72144850-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144850
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144850
    reference: chr 16
allele count: 1
allele frequency: 3.184307731499172e-5
allele num: 31404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-92A>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369-5A>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1770A>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478-5A>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414-5A>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993-5A>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669-5A>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9665
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
hgvs: c.3478-5A>T
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-72144855-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144855
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144855
    reference: chr 16
allele count: 1
allele frequency: 3.11332503113325e-5
allele num: 32120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*993G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3478G>A
  hgvsp: ENSP00000268482.3:p.Glu1160Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1765G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1414G>A
  hgvsp: ENSP00000437898.1:p.Glu472Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.669G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-87G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.369G>A
  hgvsp: ENSP00000454521.2:p.Glu124Lys
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32984
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9311
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu1160Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-72144861-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144861
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144861
    reference: chr 16
allele count: 1
allele frequency: 3.093485120336571e-5
allele num: 32326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1759C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.375C>T
  hgvsp: ENSP00000454521.2:p.Arg126Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3484C>T
  hgvsp: ENSP00000268482.3:p.Arg1162Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*999C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-81C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1420C>T
  hgvsp: ENSP00000437898.1:p.Arg474Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.675C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9269
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Arg1162Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-72144862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144862
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144862
    reference: chr 16
allele count: 10
allele frequency: 3.044510747122937e-4
allele num: 32846
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3485G>A
  hgvsp: ENSP00000268482.3:p.Arg1162His
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1421G>A
  hgvsp: ENSP00000437898.1:p.Arg474His
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.376G>A
  hgvsp: ENSP00000454521.2:p.Arg126His
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1758G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1000G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.676G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-80G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34246
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1162His
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

16-72144864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144864
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144864
    reference: chr 16
allele count: 1
allele frequency: 3.039328916175308e-5
allele num: 32902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.378C>T
  hgvsp: ENSP00000454521.2:p.Arg127Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3487C>T
  hgvsp: ENSP00000268482.3:p.Arg1163Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1002C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1423C>T
  hgvsp: ENSP00000437898.1:p.Arg475Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1756C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.678C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-78C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1163Cys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-72144867-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144867
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144867
    reference: chr 16
allele count: 3
allele frequency: 9.100285142267791e-5
allele num: 32966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-75C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3490C>T
  hgvsp: ENSP00000268482.3:p.Arg1164Trp
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1005C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1426C>T
  hgvsp: ENSP00000437898.1:p.Arg476Trp
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1753C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.681C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.381C>T
  hgvsp: ENSP00000454521.2:p.Arg128Trp
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34054
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6566
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1164Trp
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-72144874-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144874
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144874
    reference: chr 16
allele count: 1
allele frequency: 2.987214720994145e-5
allele num: 33476
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3497A>G
  hgvsp: ENSP00000268482.3:p.Lys1166Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1433A>G
  hgvsp: ENSP00000437898.1:p.Lys478Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.388A>G
  hgvsp: ENSP00000454521.2:p.Lys130Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1012A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.688A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1746A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-68A>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys1166Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-72144878-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144878
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144878
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 33512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.692G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.392G>A
  hgvsp: ENST00000567142.2:c.392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-64G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3501G>A
  hgvsp: ENST00000268482.3:c.3501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1437G>A
  hgvsp: ENST00000536867.1:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1742G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1016G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34162
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu1167Glu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

16-72144881-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144881
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144880
    reference: chr 16
allele count: 1
allele frequency: 2.965774956996263e-5
allele num: 33718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.396delG
  hgvsp: ENSP00000454521.2:p.Ala133ProfsTer48
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1020delG
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.696delG
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1738delG
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3505delG
  hgvsp: ENSP00000268482.3:p.Ala1169ProfsTer48
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1441delG
  hgvsp: ENSP00000437898.1:p.Ala481ProfsTer48
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-60delG
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8790
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2670
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala1169ProfsTer48
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: AG
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

16-72144897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144897
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144897
    reference: chr 16
allele count: 1
allele frequency: 2.95386069592958e-5
allele num: 33854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.711G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1456G>A
  hgvsp: ENSP00000437898.1:p.Glu486Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1723G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.411G>A
  hgvsp: ENSP00000454521.2:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1035G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3520G>A
  hgvsp: ENSP00000268482.3:p.Glu1174Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-45G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2284
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9788
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1174Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-72144900-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144900
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144900
    reference: chr 16
allele count: 1
allele frequency: 2.965247301624956e-5
allele num: 33724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1459G>A
  hgvsp: ENSP00000437898.1:p.Glu487Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1038G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-42G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3523G>A
  hgvsp: ENSP00000268482.3:p.Glu1175Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.414G>A
  hgvsp: ENSP00000454521.2:p.Glu139Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1720G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.714G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8448
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu1175Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-72144908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144908
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144908
    reference: chr 16
allele count: 8
allele frequency: 2.424536307431204e-4
allele num: 32996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.422G>A
  hgvsp: ENST00000567142.2:c.422G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.722G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1046G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1467G>A
  hgvsp: ENST00000536867.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3531G>A
  hgvsp: ENST00000268482.3:c.3531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-34G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1712G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32221
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3370
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala1177Ala
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-72144908-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144908
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144908
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 32996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1467G>T
  hgvsp: ENST00000536867.1:c.1467G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.422G>T
  hgvsp: ENST00000567142.2:c.422G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1046G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1712G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3531G>T
  hgvsp: ENST00000268482.3:c.3531G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.722G>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-34G>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 32221
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3370
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10980
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala1177Ala
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

16-72144914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144914
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144914
    reference: chr 16
allele count: 20
allele frequency: 6.11396429444852e-4
allele num: 32712
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3537C>T
  hgvsp: ENST00000268482.3:c.3537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.428C>T
  hgvsp: ENST00000567142.2:c.428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1706C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1052C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1473C>T
  hgvsp: ENST00000536867.1:c.1473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-28C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.728C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31743
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11725
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7830
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
hgvs: p.Ala1179Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS

16-72144917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144917
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144917
    reference: chr 16
allele count: 3
allele frequency: 9.157509157509158e-5
allele num: 32760
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3540G>A
  hgvsp: ENST00000268482.3:c.3540G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1476G>A
  hgvsp: ENST00000536867.1:c.1476G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.431G>A
  hgvsp: ENST00000567142.2:c.431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1055G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1703G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.731G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-25G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12016
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5572
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31518
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7921
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu1180Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-72144924-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144924
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144924
    reference: chr 16
allele count: 1
allele frequency: 3.133813851457223e-5
allele num: 31910
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3547C>T
  hgvsp: ENST00000268482.3:c.3547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-18C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.738C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.438C>T
  hgvsp: ENST00000567142.2:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1062C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1483C>T
  hgvsp: ENST00000536867.1:c.1483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1696C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7367
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu1183Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

16-72144927-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144927
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144927
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 30876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.741C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-15C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.441C>T
  hgvsp: ENSP00000454521.2:p.Arg148Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1486C>T
  hgvsp: ENSP00000437898.1:p.Arg496Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1693C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3550C>T
  hgvsp: ENSP00000268482.3:p.Arg1184Ter
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1065C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29631
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14378
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3360
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1184Ter
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-72144934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144934
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144934
    reference: chr 16
allele count: 1
allele frequency: 3.335334534053766e-5
allele num: 29982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.448G>A
  hgvsp: ENSP00000454521.2:p.Arg150Gln
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1072G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1493G>A
  hgvsp: ENSP00000437898.1:p.Arg498Gln
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1686G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-8G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3557G>A
  hgvsp: ENSP00000268482.3:p.Arg1186Gln
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.748G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15965
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg1186Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-72144936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144936
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144936
    reference: chr 16
allele count: 1
allele frequency: 3.359086328518643e-5
allele num: 29770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1495C>T
  hgvsp: ENSP00000437898.1:p.Arg499Trp
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1074C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3559C>T
  hgvsp: ENSP00000268482.3:p.Arg1187Trp
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.450C>T
  hgvsp: ENSP00000454521.2:p.Arg151Trp
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.750C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1684C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-6C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16254
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1187Trp
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-72144937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144937
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144937
    reference: chr 16
allele count: 2
allele frequency: 6.821282401091406e-5
allele num: 29320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1496G>A
  hgvsp: ENSP00000437898.1:p.Arg499Gln
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3560G>A
  hgvsp: ENSP00000268482.3:p.Arg1187Gln
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1075G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1683G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-5G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.751G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.451G>A
  hgvsp: ENSP00000454521.2:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27804
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16988
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26377
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg1187Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

16-72144941-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144941
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144941
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 29082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.445-1G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1679G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1079G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1500G>A
  hgvsp: ENST00000536867.1:c.1500G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3564G>A
  hgvsp: ENST00000268482.3:c.3564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.755G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.455G>A
  hgvsp: ENST00000567142.2:c.455G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
canonical: false
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27609
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27298
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: c.445-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-72144946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144946
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144946
    reference: chr 16
allele count: 5
allele frequency: 1.783675799086758e-4
allele num: 28032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1674A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1505A>G
  hgvsp: ENSP00000437898.1:p.Gln502Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.449A>G
  hgvsp: ENSP00000462397.1:p.Gln150Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3569A>G
  hgvsp: ENSP00000268482.3:p.Gln1190Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.460A>G
  hgvsp: ENSP00000454521.2:p.Gln154Arg
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1084A>G
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.760A>G
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26274
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19161
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25469
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19123
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln1190Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

16-72144953-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144953
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144953
    reference: chr 16
allele count: 1
allele frequency: 3.758550702848981e-5
allele num: 26606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1512G>C
  hgvsp: ENSP00000437898.1:p.Lys504Asn
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3576G>C
  hgvsp: ENSP00000268482.3:p.Lys1192Asn
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.456G>C
  hgvsp: ENSP00000462397.1:p.Lys152Asn
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.767G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.467G>C
  hgvsp: ENSP00000454521.2:p.Lys156Asn
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1091G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1667G>C
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys1192Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

16-72144954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144954
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144954
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 26338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1092C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.468C>T
  hgvsp: ENSP00000454521.2:p.Arg157Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.768C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.457C>T
  hgvsp: ENSP00000462397.1:p.Arg153Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1513C>T
  hgvsp: ENSP00000437898.1:p.Arg505Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3577C>T
  hgvsp: ENSP00000268482.3:p.Arg1193Cys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1666C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24718
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg1193Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

16-72144965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144965
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144965
    reference: chr 16
allele count: 5
allele frequency: 2.077965256420913e-4
allele num: 24062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.779G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.468G>C
  hgvsp: ENST00000563819.1:c.468G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1655G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1103G>C
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.479G>C
  hgvsp: ENST00000567142.2:c.479G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3588G>C
  hgvsp: ENST00000268482.3:c.3588G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1524G>C
  hgvsp: ENST00000536867.1:c.1524G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21994
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24648
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu1196Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

16-72144976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144976
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144976
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 20172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.490G>A
  hgvsp: ENSP00000454521.2:p.Arg164Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1644G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1535G>A
  hgvsp: ENSP00000437898.1:p.Arg512Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.479G>A
  hgvsp: ENSP00000462397.1:p.Arg160Lys
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1114G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.790G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3599G>A
  hgvsp: ENSP00000268482.3:p.Arg1200Lys
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17389
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2580
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1200Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

16-72144985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144985
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144985
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 17072
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3599+9C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.479+9C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1635C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1535+9C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.490+9C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1114+9C>T
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.790+9C>T
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14918
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30817
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12229
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

16-72144986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72144986
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 72144986
    reference: chr 16
allele count: 1
allele frequency: 5.996641880546894e-5
allele num: 16676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462965
  ensembl transcript: ENST00000562774
  gene symbol: DHX38
  hgvsc: ENST00000562774.1:c.313-1634G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000268482
  ensembl transcript: ENST00000268482
  gene symbol: DHX38
  hgvsc: ENST00000268482.3:c.3599+10G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462397
  ensembl transcript: ENST00000563819
  gene symbol: DHX38
  hgvsc: ENST00000563819.1:c.479+10G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000462149
  ensembl transcript: ENST00000579387
  gene symbol: DHX38
  hgvsc: ENST00000579387.1:c.*1114+10G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000437898
  ensembl transcript: ENST00000536867
  gene symbol: DHX38
  hgvsc: ENST00000536867.1:c.1535+10G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl transcript: ENST00000567552
  gene symbol: DHX38
  hgvsc: ENST00000567552.1:n.790+10G>A
  variant of: http://identifiers.org/hgnc/17211
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140829
  ensembl protein: ENSP00000454521
  ensembl transcript: ENST00000567142
  gene symbol: DHX38
  hgvsc: ENST00000567142.2:c.490+10G>A
  variant of: http://identifiers.org/hgnc/17211
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30856
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff

GenotypeQuality
all individuals: 2012
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8034
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.242e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.628814e6

QD
type: SiteQuality
SIO_000300: 2.457e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.924e1

GenotypeQuality
all individuals: 1037
bin: 7.5e0
variant carriers: 20

GenotypeQuality
all individuals: 763
bin: 5.25e1
variant carriers: 29

GenotypeQuality
all individuals: 5021
bin: 9.75e1
variant carriers: 4464

GenotypeQuality
all individuals: 957
bin: 3.25e1
variant carriers: 23

GenotypeQuality
all individuals: 27299
bin: 2.5e0
variant carriers: 13

GenotypeQuality
all individuals: 2228
bin: 6.75e1
variant carriers: 22

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 24

GenotypeQuality
all individuals: 629
bin: 7.25e1
variant carriers: 21

GenotypeQuality
all individuals: 830
bin: 4.25e1
variant carriers: 19

GenotypeQuality
all individuals: 629
bin: 7.75e1
variant carriers: 15

GenotypeQuality
all individuals: 840
bin: 4.75e1
variant carriers: 21

GenotypeQuality
all individuals: 193
bin: 9.25e1
variant carriers: 19

GenotypeQuality
all individuals: 13601
bin: 6.25e1
variant carriers: 14

European (Finnish)
type: Population
allele count: 542
allele frequency: 2.659470068694799e-1
allele num: 2038
num of homozygotes: 0

Other
type: Population
allele count: 46
allele frequency: 9.163346613545817e-2
allele num: 502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2804
allele frequency: 7.717289591016678e-2
allele num: 36334
num of homozygotes: 0

Latino
type: Population
allele count: 230
allele frequency: 7.91465932553338e-2
allele num: 2906
num of homozygotes: 0

South Asian
type: Population
allele count: 75
allele frequency: 6.420133538777606e-3
allele num: 11682
num of homozygotes: 0

East Asian
type: Population
allele count: 200
allele frequency: 8.136696501220504e-2
allele num: 2458
num of homozygotes: 0

African
type: Population
allele count: 832
allele frequency: 2.199894235854045e-1
allele num: 3782
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

FS
type: SiteQuality
SIO_000300: 4.52496e2

MQ
type: SiteQuality
SIO_000300: 5.819e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

DP
type: SiteQuality
SIO_000300: 2.182505e6

VQSLOD
type: SiteQuality
SIO_000300: -9.587e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.274e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e0

QD
type: SiteQuality
SIO_000300: 8.210000000000001e0

GenotypeQuality
all individuals: 13601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27299
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.712035610340695e-4
allele num: 11682
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.441156228492773e-4
allele num: 2906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.182505e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.274e0

FS
type: SiteQuality
SIO_000300: 4.52496e2

QD
type: SiteQuality
SIO_000300: 8.210000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -9.587e2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

MQ
type: SiteQuality
SIO_000300: 5.819e1

GenotypeQuality
all individuals: 877
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7575
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6006
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036560184622859e-5
allele num: 65864
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.953918865695155e-4
allele num: 10156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.332e1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.802e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 7.089e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 1.877795e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.151e0

GenotypeQuality
all individuals: 5774
bin: 9.75e1
variant carriers: 676

GenotypeQuality
all individuals: 2740
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 753
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 823
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 482
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7582
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1624
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 676
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 870
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2461
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 773
bin: 5.25e1
variant carriers: 2

Latino
type: Population
allele count: 8
allele frequency: 7.006480994920302e-4
allele num: 11418
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.681818181818182e-3
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 49
allele frequency: 8.134130146082337e-3
allele num: 6024
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.235635734585444e-4
allele num: 16186
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.352349777881693e-4
allele num: 8554
num of homozygotes: 0

African
type: Population
allele count: 167
allele frequency: 1.644672050423478e-2
allele num: 10154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 471
allele frequency: 7.150664966296229e-3
allele num: 65868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.794e0

VQSLOD
type: SiteQuality
SIO_000300: -1.243e2

MQ
type: SiteQuality
SIO_000300: 5.779e1

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

FS
type: SiteQuality
SIO_000300: 3.52953e2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.924e0

DP
type: SiteQuality
SIO_000300: 1.875383e6

QD
type: SiteQuality
SIO_000300: 7.23e0

GenotypeQuality
all individuals: 6531
bin: 6.75e1
variant carriers: 11

GenotypeQuality
all individuals: 867
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 311
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 421
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 886
bin: 4.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1101
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2024
bin: 2.25e1
variant carriers: 14

GenotypeQuality
all individuals: 5225
bin: 9.75e1
variant carriers: 3676

GenotypeQuality
all individuals: 926
bin: 8.25e1
variant carriers: 14

GenotypeQuality
all individuals: 871
bin: 3.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1301
bin: 5.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1957
bin: 7.25e1
variant carriers: 11

GenotypeQuality
all individuals: 400
bin: 8.75e1
variant carriers: 13

European (Finnish)
type: Population
allele count: 480
allele frequency: 9.937888198757763e-2
allele num: 4830
num of homozygotes: 0

South Asian
type: Population
allele count: 61
allele frequency: 3.816793893129771e-3
allele num: 15982
num of homozygotes: 0

African
type: Population
allele count: 637
allele frequency: 6.966316710411198e-2
allele num: 9144
num of homozygotes: 0

Latino
type: Population
allele count: 205
allele frequency: 1.884191176470588e-2
allele num: 10880
num of homozygotes: 0

East Asian
type: Population
allele count: 175
allele frequency: 2.08036138849263e-2
allele num: 8412
num of homozygotes: 0

Other
type: Population
allele count: 38
allele frequency: 4.75e-2
allele num: 800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2229
allele frequency: 3.565829467285234e-2
allele num: 62510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.805e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.96e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.719e2

FS
type: SiteQuality
SIO_000300: 2.40278e2

QD
type: SiteQuality
SIO_000300: 1.12e1

MQ
type: SiteQuality
SIO_000300: 5.847e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e0

DP
type: SiteQuality
SIO_000300: 1.689114e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.229e0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34644
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2353
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1195
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 763
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7821
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2715
bin: 9.75e1
variant carriers: 248

GenotypeQuality
all individuals: 2401
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.362862010221465e-3
allele num: 5870
num of homozygotes: 0

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

African
type: Population
allele count: 100
allele frequency: 1.029442042413012e-2
allele num: 9714
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 150
allele frequency: 2.320329177365963e-3
allele num: 64646
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.567e0

DP
type: SiteQuality
SIO_000300: 1.61688e6

MQ
type: SiteQuality
SIO_000300: 5.816e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.325e0

VQSLOD
type: SiteQuality
SIO_000300: -2.952e1

FS
type: SiteQuality
SIO_000300: 1.65676e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

QD
type: SiteQuality
SIO_000300: 1.387e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.117e0

GenotypeQuality
all individuals: 756
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34726
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 411
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2393
bin: 9.75e1
variant carriers: 42

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.658982802780827e-4
allele num: 5466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.219409282700422e-4
allele num: 63990
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 1.697072549851506e-3
allele num: 9428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1143e2

MQ
type: SiteQuality
SIO_000300: 5.794e1

QD
type: SiteQuality
SIO_000300: 1.571e1

VQSLOD
type: SiteQuality
SIO_000300: -6.486e1

MQRankSum
type: SiteQuality
SIO_000300: -2.471e0

DP
type: SiteQuality
SIO_000300: 1.593794e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.841e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.242e0

GenotypeQuality
all individuals: 152
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 9.75e1
variant carriers: 42

GenotypeQuality
all individuals: 2224
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2575
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 769
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.841620626151013e-4
allele num: 5430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 4.052874423244793e-4
allele num: 64152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 1.689545934530095e-3
allele num: 9470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.311e0

DP
type: SiteQuality
SIO_000300: 1.591278e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.702e0

VQSLOD
type: SiteQuality
SIO_000300: -3.225e1

QD
type: SiteQuality
SIO_000300: 1.635e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 7.5767e1

MQ
type: SiteQuality
SIO_000300: 5.805e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.258e0

GenotypeQuality
all individuals: 1157
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5918
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526624328285296e-5
allele num: 65504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.625e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.55e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-1

DP
type: SiteQuality
SIO_000300: 1.636939e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3623
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7369
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 5.680248088673278e-4
allele num: 65138
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.007226013649137e-4
allele num: 9964
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.138731952291275e-4
allele num: 15930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.368647100930566e-4
allele num: 5588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.898380494749955e-5
allele num: 11238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.623983e6

MQ
type: SiteQuality
SIO_000300: 5.914e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

QD
type: SiteQuality
SIO_000300: 1.195e1

GenotypeQuality
all individuals: 172
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.709048221058335e-4
allele num: 11074
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

FS
type: SiteQuality
SIO_000300: 6.117e0

DP
type: SiteQuality
SIO_000300: 1.584305e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

QD
type: SiteQuality
SIO_000300: 2.843e1

MQ
type: SiteQuality
SIO_000300: 5.923e1

VQSLOD
type: SiteQuality
SIO_000300: -1.543e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

GenotypeQuality
all individuals: 1001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6928
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1721
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2719
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.03476821192053e-4
allele num: 9664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.889e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.546402e6

FS
type: SiteQuality
SIO_000300: 1.048e0

QD
type: SiteQuality
SIO_000300: 1.499e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.271e-1

GenotypeQuality
all individuals: 505
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.51890482398957e-5
allele num: 15340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10792
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.315e0

QD
type: SiteQuality
SIO_000300: 1.019e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e0

DP
type: SiteQuality
SIO_000300: 1.521151e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1642
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 882
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8717
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 644

GenotypeQuality
all individuals: 533
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 948
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 190
allele frequency: 1.249506773641983e-2
allele num: 15206
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 9.455370650529501e-4
allele num: 5288
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 6.157635467980296e-3
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 389
allele frequency: 6.200784263716645e-3
allele num: 62734
num of homozygotes: 1

African
type: Population
allele count: 15
allele frequency: 1.574307304785894e-3
allele num: 9528
num of homozygotes: 0

Latino
type: Population
allele count: 45
allele frequency: 4.207180254300673e-3
allele num: 10696
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.496004e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

FS
type: SiteQuality
SIO_000300: 2.065e0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10696
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62734
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.382e1

DP
type: SiteQuality
SIO_000300: 1.496004e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

FS
type: SiteQuality
SIO_000300: 2.065e0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
all individuals: 1218
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1579
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28559
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5562
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15184
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.597597213790459e-5
allele num: 62594
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10660
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.279e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.066e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.444e0

QD
type: SiteQuality
SIO_000300: 1.543e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.483996e6

GenotypeQuality
all individuals: 24448
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1315
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 670
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 2038
bin: 9.75e1
variant carriers: 585

GenotypeQuality
all individuals: 634
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2414
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 638
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1653
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1131
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1724
bin: 5.25e1
variant carriers: 9

GenotypeQuality
all individuals: 330
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1703
bin: 5.75e1
variant carriers: 6

East Asian
type: Population
allele count: 1
allele frequency: 1.292323597828896e-4
allele num: 7738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 374
allele frequency: 6.436734131901418e-3
allele num: 58104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.616805170821791e-4
allele num: 4332
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 5.494505494505495e-3
allele num: 728
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.743088334457182e-5
allele num: 14830
num of homozygotes: 0

African
type: Population
allele count: 282
allele frequency: 3.381294964028777e-2
allele num: 8340
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.0e-4
allele num: 10000
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.63e0

VQSLOD
type: SiteQuality
SIO_000300: -6.166e2

FS
type: SiteQuality
SIO_000300: 3.6186e2

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

DP
type: SiteQuality
SIO_000300: 1.496156e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.669e0

MQ
type: SiteQuality
SIO_000300: 5.53e1

QD
type: SiteQuality
SIO_000300: 3.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.221e0

GenotypeQuality
all individuals: 1227
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2564
bin: 9.75e1
variant carriers: 498

GenotypeQuality
all individuals: 734
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1374
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 256
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 336
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2434
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4912
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 5.154639175257732e-3
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 317
allele frequency: 5.180246429388503e-3
allele num: 61194
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.256597134958532e-4
allele num: 7958
num of homozygotes: 0

African
type: Population
allele count: 206
allele frequency: 2.24694589877836e-2
allele num: 9168
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.152823920265781e-4
allele num: 4816
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.15989e2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.375e0

VQSLOD
type: SiteQuality
SIO_000300: -2.242e2

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.027e0

QD
type: SiteQuality
SIO_000300: 4.48e0

MQ
type: SiteQuality
SIO_000300: 5.572e1

DP
type: SiteQuality
SIO_000300: 1.439621e6

GenotypeQuality
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bin: 7.5e0
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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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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variant carriers: 1419

GenotypeQuality
all individuals: 4832
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 479
bin: 5.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1256
allele frequency: 2.048204559538176e-2
allele num: 61322
num of homozygotes: 14

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

European (Finnish)
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allele count: 31
allele frequency: 6.13132911392405e-3
allele num: 5056
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.668001067520683e-3
allele num: 14988
num of homozygotes: 2

Other
type: Population
allele count: 7
allele frequency: 8.883248730964468e-3
allele num: 788
num of homozygotes: 0

Latino
type: Population
allele count: 63
allele frequency: 6.069364161849711e-3
allele num: 10380
num of homozygotes: 0

African
type: Population
allele count: 79
allele frequency: 8.551634552933535e-3
allele num: 9238
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.494e0

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

DP
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SIO_000300: 1.430308e6

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

InbreedingCoeff
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SIO_000300: 4.8e-3

MQ
type: SiteQuality
SIO_000300: 5.876e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

QD
type: SiteQuality
SIO_000300: 1.465e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.098659635245001e-4
allele num: 9102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4774
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 5.543e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.360461e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: -4.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.546e0

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
all individuals: 3891
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.665334399147349e-5
allele num: 60048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.521e1

QD
type: SiteQuality
SIO_000300: 1.203e1

VQSLOD
type: SiteQuality
SIO_000300: -3.778e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.348442e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.398e0

GenotypeQuality
all individuals: 3482
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 3847
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.311989401633915e-4
allele num: 9058
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.428e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

FS
type: SiteQuality
SIO_000300: 7.75e-1

DP
type: SiteQuality
SIO_000300: 1.337803e6

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.926e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 573
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 543
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.677627164139042e-5
allele num: 59608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.310413e6

QD
type: SiteQuality
SIO_000300: 1.364e1

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.29366106080207e-4
allele num: 7730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4738
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.310413e6

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

BaseQRankSum
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.682651859330305e-5
allele num: 59430
num of homozygotes: 0

East Asian
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South Asian
type: Population
allele count: 0
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African
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allele count: 5
allele frequency: 5.575379125780553e-4
allele num: 8968
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.301247e6

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.805e1

MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.687991627561527e-5
allele num: 59242
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14632
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.735e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
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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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.698254194687861e-5
allele num: 58884
num of homozygotes: 0

Other
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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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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.341e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

DP
type: SiteQuality
SIO_000300: 1.265235e6

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4620
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58696
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 754
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South Asian
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allele frequency: 6.894649751792609e-5
allele num: 14504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.262324e6

QD
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MQ
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.388e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.71e-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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8850
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14524
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.333333333333333e-3
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.191205499965965e-4
allele num: 58764
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.251788e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.646e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-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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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: 746
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.721822376803609e-5
allele num: 58078
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4548
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.031991744066047e-4
allele num: 9690
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14454
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.993e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.49e-1

DP
type: SiteQuality
SIO_000300: 1.204481e6

GenotypeQuality
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variant carriers: 1

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

South Asian
type: Population
allele count: 39
allele frequency: 2.729181245626312e-3
allele num: 14290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.342e1

DP
type: SiteQuality
SIO_000300: 1.162543e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.845e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-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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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.830161054172767e-5
allele num: 54640
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4160
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.082e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

FS
type: SiteQuality
SIO_000300: 7.912e0

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.84e-1

DP
type: SiteQuality
SIO_000300: 1.088412e6

QD
type: SiteQuality
SIO_000300: 5.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-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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variant carriers: 0

African
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allele count: 1
allele frequency: 1.222792858889704e-4
allele num: 8178
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6872
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54150
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ClippingRankSum
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

BaseQRankSum
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QD
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VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
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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
allele num: 698
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 2.276867030965392e-4
allele num: 8784
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53868
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

European (Non-Finnish)
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allele count: 3
allele frequency: 5.637614161686774e-5
allele num: 53214
num of homozygotes: 0

South Asian
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allele frequency: 1.473622163277336e-4
allele num: 13572
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Latino
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allele frequency: 4.634994206257242e-4
allele num: 8630
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African
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
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allele num: 700
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.78960133393967e-5
allele num: 52776
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.364087301587302e-3
allele num: 8064
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.481920569057498e-4
allele num: 13496
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.068111e6

FS
type: SiteQuality
SIO_000300: 2.445e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.372e1

MQ
type: SiteQuality
SIO_000300: 5.739e1

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 2001
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.993461446455626e-5
allele num: 50164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13080
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -7.677e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

DP
type: SiteQuality
SIO_000300: 1.061856e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.807e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.386e0

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.900142202559646e-5
allele num: 12658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1740
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.763e1

MQRankSum
type: SiteQuality
SIO_000300: -2.117e0

QD
type: SiteQuality
SIO_000300: 5.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.94e-2

DP
type: SiteQuality
SIO_000300: 4.99163e5

VQSLOD
type: SiteQuality
SIO_000300: -3.189e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.799e0

FS
type: SiteQuality
SIO_000300: 2.596e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.376e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 756
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13028
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.427e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

DP
type: SiteQuality
SIO_000300: 5.28206e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 1911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3199
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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
all individuals: 821
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.347593582887701e-4
allele num: 1870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.13e-1

DP
type: SiteQuality
SIO_000300: 5.49321e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.41e-1

GenotypeQuality
all individuals: 441
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 951
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variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 4.25e1
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GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8017
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variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 1.4058106841612e-3
allele num: 2134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14918
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.11512e5

FS
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.340662287169862e-4
allele num: 14918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

FS
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 6.11512e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3822
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 6.635700066357e-5
allele num: 15070
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.14433e5

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.268e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-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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bin: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.821282401091405e-4
allele num: 1466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15472
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.23858e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 77
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.747638326585695e-4
allele num: 1482
num of homozygotes: 0

African
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2200
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.043e0

DP
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15826
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2244
num of homozygotes: 0

Latino
type: Population
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allele frequency: 6.46830530401035e-4
allele num: 1546
num of homozygotes: 0

South Asian
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allele count: 9
allele frequency: 1.050420168067227e-3
allele num: 8568
num of homozygotes: 0

QD
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SIO_000300: 9.970000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.24e-1

FS
type: SiteQuality
SIO_000300: 9.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

DP
type: SiteQuality
SIO_000300: 6.32011e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2254
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1532
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 6.29643621710112e-5
allele num: 15882
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.32712e5

FS
type: SiteQuality
SIO_000300: 2.059e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.002e0

VQSLOD
type: SiteQuality
SIO_000300: 2.86e-1

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 1
allele frequency: 6.485084306095979e-4
allele num: 1542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 6.28140703517588e-5
allele num: 15920
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.002e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

FS
type: SiteQuality
SIO_000300: 1.462e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.05e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

DP
type: SiteQuality
SIO_000300: 6.34832e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 1
allele frequency: 6.170554115759595e-5
allele num: 16206
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8690
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1604
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 1.11e1

MQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.92e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.59e-1

FS
type: SiteQuality
SIO_000300: 2.966e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

DP
type: SiteQuality
SIO_000300: 6.35353e5

GenotypeQuality
all individuals: 31635
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8662
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GenotypeQuality
all individuals: 160
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.521e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 5.07e0

DP
type: SiteQuality
SIO_000300: 6.3555e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 225
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2330
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.097560975609756e-5
allele num: 16400
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

QD
type: SiteQuality
SIO_000300: 4.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

DP
type: SiteQuality
SIO_000300: 6.37119e5

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 496
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South Asian
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allele count: 1
allele frequency: 1.148897058823529e-4
allele num: 8704
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Other
type: Population
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.419e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2306
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.180469715698393e-4
allele num: 1618
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
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Other
type: Population
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allele num: 278
num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
type: Population
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allele frequency: 0.0e0
allele num: 266
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European (Non-Finnish)
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allele count: 7
allele frequency: 4.37883147754285e-4
allele num: 15986
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

QD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 3818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2232
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

FS
type: SiteQuality
SIO_000300: 4.082e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.214e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-2

DP
type: SiteQuality
SIO_000300: 6.18969e5

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 1

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

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 243
bin: 7.25e1
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GenotypeQuality
all individuals: 236
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.153136531365314e-4
allele num: 8672
num of homozygotes: 0

East Asian
type: Population
allele count: 14
allele frequency: 6.493506493506494e-3
allele num: 2156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 2.525571410531633e-4
allele num: 15838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.55307994757536e-4
allele num: 1526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

DP
type: SiteQuality
SIO_000300: 6.1249e5

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

QD
type: SiteQuality
SIO_000300: 1.047e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.581e0

GenotypeQuality
all individuals: 546
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 237
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.297016861219196e-3
allele num: 1542
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 4.699248120300752e-4
allele num: 2128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.46e-2

QD
type: SiteQuality
SIO_000300: 8.9e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 6.08857e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.06e-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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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2058
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

DP
type: SiteQuality
SIO_000300: 5.93079e5

QD
type: SiteQuality
SIO_000300: 1.175e1

VQSLOD
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.316e0

FS
type: SiteQuality
SIO_000300: 1.131e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.947e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 947
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 990
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GenotypeQuality
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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: 6966
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14730
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.644e0

DP
type: SiteQuality
SIO_000300: 5.8111e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.37e-1

FS
type: SiteQuality
SIO_000300: 7.512e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.98e-2

QD
type: SiteQuality
SIO_000300: 2.892e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 6743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 430
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GenotypeQuality
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GenotypeQuality
all individuals: 858
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GenotypeQuality
all individuals: 139
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GenotypeQuality
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GenotypeQuality
all individuals: 2934
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GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 211
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14240
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.177578897786152e-4
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3448
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.838e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.21e-2

FS
type: SiteQuality
SIO_000300: 3.634e0

VQSLOD
type: SiteQuality
SIO_000300: -2.793e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

DP
type: SiteQuality
SIO_000300: 5.65624e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

QD
type: SiteQuality
SIO_000300: 1.152e1

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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14146
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.446623093681918e-4
allele num: 1836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.28e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

DP
type: SiteQuality
SIO_000300: 5.63435e5

FS
type: SiteQuality
SIO_000300: 3.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.306e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.592356687898089e-3
allele num: 1256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.34e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 2.709e1

DP
type: SiteQuality
SIO_000300: 5.55727e5

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 6.816e0

VQSLOD
type: SiteQuality
SIO_000300: -2.128e0

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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GenotypeQuality
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GenotypeQuality
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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: 830
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3356
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1218
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.169e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.36e-2

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.682e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.306e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13172
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 3.037667071688943e-3
allele num: 1646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1154
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.34557e5

FS
type: SiteQuality
SIO_000300: 4.472e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

GenotypeQuality
all individuals: 538
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20892
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23688
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3014
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1060
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.240079365079365e-4
allele num: 8064
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.632e0

QD
type: SiteQuality
SIO_000300: 6.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.97e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 5.13889e5

VQSLOD
type: SiteQuality
SIO_000300: -1.258e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2629
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23456
bin: 2.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1434
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.647e1

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.1142e5

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4989
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 9.75e1
variant carriers: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1170
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 1.445086705202312e-3
allele num: 2768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11132
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.68e-2

QD
type: SiteQuality
SIO_000300: 1.38e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.09e-1

DP
type: SiteQuality
SIO_000300: 4.73113e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 4.634e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1748
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3015
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6840
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9146
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.63e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.07271e5

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 6.292e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.599e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 6.62e0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2569
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 854
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1942
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.236e-1

QD
type: SiteQuality
SIO_000300: 1.047e1

DP
type: SiteQuality
SIO_000300: 3.5814e5

FS
type: SiteQuality
SIO_000300: 1.129e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2714
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 116
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.607717041800643e-4
allele num: 6220
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.29e-2